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| Sponsor: | University of Missouri-Columbia |
|---|---|
| Information provided by: | University of Missouri-Columbia |
| ClinicalTrials.gov Identifier: | NCT00574444 |
Purpose
We propose a phase I study of laparoscopic assisted, transvaginal peritoneoscopy by using flexible endoscopy in female patients with pelvic pain. It is designed as a hybrid procedure with laparoscopy using one port for adequate safety with the ultimate goal in the future that transvaginal NOTES can replace therapeutic pelviscopy for this indication. The standard number of port sites for diagnostic laparoscopy is 2-3. By reducing the number and size of laparoscopic port, patients should already experience benefits from this hybrid procedure.
| Condition | Intervention | Phase |
|---|---|---|
|
Pelvic Pain |
Procedure: transvaginal diagnostic peritoneoscopy |
Phase I |
| Study Type: | Interventional |
| Study Design: | Diagnostic, Non-Randomized, Open Label, Single Group Assignment |
| Official Title: | Laparoscopic Assisted Transvaginal Endoscopic Diagnostic Peritoneoscopy in Women With Pelvic Pain |
| Estimated Enrollment: | 25 |
| Study Start Date: | January 2008 |
| Estimated Study Completion Date: | January 2010 |
| Estimated Primary Completion Date: | January 2010 (Final data collection date for primary outcome measure) |
Approximately 50% of patients with chronic pelvic pain will have a normal laparoscopy. The vast majority of women with endometriosis, chronic pelvic pain and absence of ovarian endometriomata determined by ultrasound will have revised ASRM Stage I or II (peritoneal) disease with preservation of the posterior cul-de-sac. This sparing of the posterior cul-de-sac may offer a preferable route of entry for endoscopic surgery compared to the current standard of care.
Despite all the advantages of laparoscopic surgery, it is not free of risks and pain, and creates scars, which themselves are associated with complications such as abdominal wall hernias and adhesions.
Within this scenario, a new surgical procedure has emerged, called natural orifice transluminal endoscopic surgery (NOTES). This technique uses existing orifices of the body for introducing optical systems and surgical instruments into the peritoneal cavity by avoiding penetration of the abdominal wall. The expectations are no postoperative pain, optimal cosmesis without any visable scars and shorter recovery similar to therapeutic endoscopy.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Contact: Klaus Thaler, MD | 573-882-9041 | thalerk@health.missouri.edu |
| Contact: Brent Miedema, MD | 573-882-9041 | miedemab@health.missouri.edu |
| United States, Missouri | |
| University of Missouri Columbia | Recruiting |
| Columbia, Missouri, United States, 65212 | |
| Contact: Kelly M Sullivan, RN 573-884-7211 sullivankm@health.missouri.edu | |
| Principal Investigator: | Klaus Thaler, MD | Dept. of General Surgery at UMHC |
More Information
| Responsible Party: | Department of General Surgery at University of Missouri, Columbia ( Klaus Thaler, MD ) |
| Study ID Numbers: | 1096837 |
| Study First Received: | December 13, 2007 |
| Last Updated: | December 2, 2008 |
| ClinicalTrials.gov Identifier: | NCT00574444 History of Changes |
| Health Authority: | United States: Institutional Review Board |
|
transvaginal peritoneoscopy |
|
Signs and Symptoms Pelvic Pain Pain |