Two Different Surgical Techniques on Postoperative Circumcision Pain

This study is not yet open for participant recruitment.
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
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 April 17, 2014