Two Different Surgical Techniques on Postoperative Circumcision Pain

This study is not yet open for participant recruitment. (see Contacts and Locations)
Verified July 2013 by Diskapi Yildirim Beyazit Education and Research Hospital
Sponsor:
Information provided by (Responsible Party):
Reyhan Polat, Diskapi Yildirim Beyazit Education and Research Hospital
ClinicalTrials.gov Identifier:
NCT01909765
First received: July 18, 2013
Last updated: July 26, 2013
Last verified: July 2013
  Purpose

To compare the effect of two different surgical techniques, the dorsal slit and double incision technique, on postoperative pain.


Condition Intervention Phase
Postoperative Pain
Other: Dorsal slit
Other: Double incision
Phase 4

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Investigator, Outcomes Assessor)
Official Title: Comparison of Two Different Circumcision Surgical Technique on Postoperative Pain

Resource links provided by NLM:


Further study details as provided by Diskapi Yildirim Beyazit Education and Research Hospital:

Primary Outcome Measures:
  • To asses postoperative pain scores on Modified Objective Assessment Scale (MOAS) [ Time Frame: Postoperative first two hours ] [ Designated as safety issue: No ]

Estimated Enrollment: 30
Study Start Date: July 2013
Estimated Study Completion Date: August 2013
Estimated Primary Completion Date: August 2013 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: Dorsal slite
Skin and mucosa insicion made together
Other: Dorsal slit
Skin and mucosa incision made together
Experimental: Double incision
Skin and mucosa incision made separately
Other: Double incision
Skin and mucosa incision made separately
Other Name: Surgical technique

Detailed Description:

Two different circumcision techniques result in different kinds of pain.This research aims determine which is more beneficial to the patient.

  Eligibility

Ages Eligible for Study:   2 Years to 14 Years
Genders Eligible for Study:   Male
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Children

Exclusion Criteria:

  • Patients with any bleeding
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01909765

Locations
Turkey
Diskapi Yildirim Beyazit Education and Research Hospital Not yet recruiting
Ankara, Turkey, 06610
Contact: Reyhan Polat, MD    +905326734310    reyhanp9@gmail.com   
Principal Investigator: Reyhan Polat, MD         
Sponsors and Collaborators
Diskapi Yildirim Beyazit Education and Research Hospital
Investigators
Principal Investigator: Reyhan Polat, MD Yildirim Beyazit Education and Research Hospital
  More Information

No publications provided

Responsible Party: Reyhan Polat, Medical Doctor, Diskapi Yildirim Beyazit Education and Research Hospital
ClinicalTrials.gov Identifier: NCT01909765     History of Changes
Other Study ID Numbers: Circumcicsion
Study First Received: July 18, 2013
Last Updated: July 26, 2013
Health Authority: Turkey: Ministry of Health

Keywords provided by Diskapi Yildirim Beyazit Education and Research Hospital:
Circumcision
postoperative pain

Additional relevant MeSH terms:
Pain, Postoperative
Postoperative Complications
Pathologic Processes
Pain
Signs and Symptoms

ClinicalTrials.gov processed this record on July 28, 2014