Comparison of Surgical Approach to Endoscopic Pituitary Adenoma Resection
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Purpose
The purpose of this study is to determine if there is a significant difference in sinonasal disease specific quality of life and utility scores between patients undergoing the posterior septectomy or Stamm approach during endoscopic pituitary adenoma resection.
| Condition | Intervention |
|---|---|
|
Pituitary Adenoma Posterior Septectomy Stamm Approach Quality of Life |
Procedure: Stamm Approach Procedure: Posterior Septectomy |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Single Blind (Subject) Primary Purpose: Treatment |
| Official Title: | Comparison of the Posterior Septectomy and Stamm Approach to Endoscopic Pituitary Adenoma Resection: A Randomized, Single-blind Trial |
- Change in Quality of Life [ Time Frame: Pre-operative and Post-operative (2 weeks, 6 weeks, 3 months and 6 months) ] [ Designated as safety issue: No ]To determine the change in quality of life scores between the two groups at 2 weeks, 6 weeks, 3 months and 6 months using the anterior skull base nasal inventory questionnaire, the SinoNasal outcome test-22 questionnaire and the EQ-5D questionnaire.
- Change in Symptom Score [ Time Frame: Pre-operative and Post-operative (2 weeks, 6 weeks, 3 months and 6 months) ] [ Designated as safety issue: No ]To determine the change in symptom score between the two groups at 2 weeks, 6 weeks, 3 months and 6 months using the VAS Nasal Symptom score.
- Change in Utility Score [ Time Frame: Pre-operative and Post-operative (2 weeks, 6 weeks, 3 months and 6 months) ] [ Designated as safety issue: No ]To determine the change in utility score between the two groups at 2 weeks, 6 weeks, 3 months and 6 months.
- Change in Endoscopic Sinus Score [ Time Frame: Pre-operative and Post-operative (2 weeks, 6 weeks, 3 months and 6 months) ] [ Designated as safety issue: No ]To determine the change in endoscopic sinus score between the two groups at 2 weeks, 6 weeks, 3 months and 6 months using the endoscopic grading - Using both the Lund-Kennedy and POSE endoscopic scoring system.
- Change in Olfaction [ Time Frame: Pre-operative and Post-operative (6 months) ] [ Designated as safety issue: No ]To determine the change in olfaction between the two groups at 6 months using the Smell Identification Test (SIT).
| Estimated Enrollment: | 55 |
| Study Start Date: | September 2012 |
| Estimated Study Completion Date: | June 2014 |
| Estimated Primary Completion Date: | December 2013 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Active Comparator: Posterior Septectomy
Patient will be randomized to a study arm. The patient will be blinded to the approach. The surgeon will have performed at least 10 procedures previous for each approach. The surgeon will maintain the following surgical practives: preservation of both middle turbinates, preservation of one superior turbinate (to minimize olfactory injury), elevation of a nasoseptal flap, the use of a combination of gelform, surgicel and nasapore dissolvable spacer placed within the surgical defect. These practices are all standard of care. Patient will start Neilmed high volume low pressure saline irrigation three times daily starting on post operative day five. Patients will receive prophylactic antibiotics for fourteen days post operatively.
|
Procedure: Posterior Septectomy |
|
Experimental: Stamm Approach
Patient will be randomized a study arm. The patient will be blinded to the approach. The surgeon will have performed at least 10 procedures previous for each approach. The surgeon will maintain the following surgical practives: preservation of both middle turbinates, preservation of one superior turbinate (to minimize olfactory injury), elevation of a nasoseptal flap, the use of a combination of gelform, surgicel and nasapore dissolvable spacer placed within the surgical defect. These practices are all standard of care. Patient will start Neilmed high volume low pressure saline irrigation three times daily starting on post operative day five. Patients will receive prophylactic antibiotics for fourteen days post operatively.
|
Procedure: Stamm Approach |
Detailed Description:
Pituitary adenoma's represent 10 to 25% of all central nervous system (CNS) neoplasms and have an estimated population prevalence of 94 per 100,000. Asymptomatic adenomas go largely undetected since there is no screening protocol implemented with the purpose for early identification. Asymptomatic adenomas can be detected incidentally on CNS imaging for other indications in approximately 10% of studies and rarely require surgical intervention. In 2011, the Endocrine Society published practice guidelines on the management of pituitary incidentalomas and provided the surgical indications. Incidental microadenoma's (< 10 mm) rarely need surgical intervention, however, incidental macroadenoma's (> 10 mm) often required surgical resection due to the proximity of the optic nerves and chiasm.
Most symptomatic pituitary adenomas require transnasal transsphenoid surgical resection. Due to the potential for hormone secretion and location to vital structures such as the optic chiasm/nerves, carotid artery, and cavernous sinus, management of symptomatic pituitary adenomas often require a multi-disciplinary team involving neurosurgery, otolaryngology, neuroophthalmology, and endocrinology. Traditionally the microscope was used for visualization during pituitary tumor surgery, however with recent technologic advances, the endoscopic approach has largely replaced the microscopic approach. A recent systematic review and meta-analysis compared the microscopic and endoscopic approaches and have demonstrated that the endoscopic approach results in a significant reduction in the rate of cerebral spinal fluid (CSF) leak, improved tumor resection, improved patient comfort, and reduced hospital length of stay. Furthermore, the endoscopic approach appears to provide an overall cost savings compared to the microscopic approach.
Several recent studies have demonstrated that the endoscopic approach for pituitary adenoma resection results in improved disease-specific quality of life (QoL) and general QoL. All studies have utilized the posterior septectomy approach which involves removing the posterior nasal septum to create a common posterior nasal cavity. The open posterior nasal cavity provides excellent surgical access to the sphenoid sinus and pituitary gland. Disadvantages of the posterior septectomy approach include the permanent posterior septal perforation which may predispose to postoperative crusting and epistaxis. A recent article by Stamm et al. described a novel endoscopic approach whereby the posterior septal mucosa is preserved while still providing excellent access to the sphenoid. The primary advantage of this approach is preventing a posterior septal defect, however disadvantages include being a more challenging technique and the potential for reduced surgical visualization. Furthermore, there is still a risk of a septal perforation due to intraoperative trauma and significant postoperative crusting which often develops along the surface of the healing septal mucosa. Both endoscopic approaches have inherent advantages and disadvantages and there has been no study comparing these approaches. Surgeons performing endoscopic pituitary tumor resections utilize both approaches and neither is considered the standard of care.
The purpose of this randomized, single-blinded study is to determine the clinical outcomes between the posterior septectomy and Stamm approach for endoscopic pituitary adenoma resection. We hypothesize that there will be no difference in disease-specific QoL and general QoL between the two surgical approaches.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Age > 18 years old
Diagnosis of a pituitary adenoma requiring resection defined as pituitary lesion with any of the following:
- Neuroimaging or clinical evidence of apoplexy
- Decline in central visual acuity worse than (best-corrected) Snellen equivalent of 20/25 in either eye
- clinically significant visual field loss as determined by Humphrey or Goldmann perimetry
- Clinically significant cranial nerve deficit
- Clinically relevant neuroendocrine deficit
- Intolerance of optimal medical management
- Patient electing endoscopic resection approach
Exclusion Criteria:
- Concurrent chronic rhinosinusitis
- Revision pituitary adenoma resections
- Severe medical co-morbidities with the inability to undergo general anesthesia
Contacts and Locations| Contact: Luke Rudmik, MD | 403-837-5853 | lukerudmik@gmail.com |
| Contact: Kristine Smith, MD | 587-228-3391 | kasmi@ucalgary.ca |
| Canada, Alberta | |
| University of Calgary | Recruiting |
| Calgary, Alberta, Canada | |
| Contact: Luke Rudmik, MD lukerudmik@gmail.com | |
| Contact: Kristine Smith, MD 587-228-3391 kasmi@ucalgary.ca | |
| Principal Investigator: Luke Rudmik, MD | |
| Principal Investigator: Brad Mechor, MD | |
| Sub-Investigator: Kristine Smith, MD | |
| Sub-Investigator: Fiona Costello, MD | |
| Sub-Investigator: Alim Mitha, MD,MSc | |
| Sub-Investigator: Yves Starreveld, MD, PhD | |
| Principal Investigator: | Luke Rudmik, MD | University of Calgary |
More Information
Publications:
| Responsible Party: | Dr. Luke Rudmik, Principal Investigator, University of Calgary |
| ClinicalTrials.gov Identifier: | NCT01689064 History of Changes |
| Other Study ID Numbers: | E-24588 |
| Study First Received: | September 17, 2012 |
| Last Updated: | September 17, 2012 |
| Health Authority: | Canada: Ethics Review Committee |
Additional relevant MeSH terms:
|
Pituitary Neoplasms Adenoma Neoplasms, Glandular and Epithelial Neoplasms by Histologic Type Neoplasms Endocrine Gland Neoplasms Neoplasms by Site Hypothalamic Neoplasms Supratentorial Neoplasms |
Brain Neoplasms Central Nervous System Neoplasms Nervous System Neoplasms Brain Diseases Central Nervous System Diseases Nervous System Diseases Hypothalamic Diseases Pituitary Diseases Endocrine System Diseases |
ClinicalTrials.gov processed this record on May 21, 2013