Two Different Surgical Techniques on Postoperative Circumcision Pain

July 26, 2013 updated by: Reyhan Polat, Diskapi Yildirim Beyazit Education and Research Hospital

Comparison of Two Different Circumcision Surgical Technique on Postoperative Pain

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

Study Overview

Status

Unknown

Conditions

Intervention / Treatment

Detailed Description

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

Study Type

Interventional

Enrollment (Anticipated)

30

Phase

  • Phase 4

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Turkey
      • Ankara, Turkey, 06610
        • Diskapi Yildirim Beyazit Education and Research Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

2 years to 14 years (Child)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  • Children

Exclusion Criteria:

  • Patients with any bleeding

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
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 Names:
  • Surgical technique

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
To asses postoperative pain scores on Modified Objective Assessment Scale (MOAS)
Time Frame: Postoperative first two hours
Postoperative first two hours

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Diskapi Yildirim Beyazit Education and Research Hospital

Investigators

  • Principal Investigator: Reyhan Polat, MD, Yildirim Beyazit Education and Research Hospital

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

July 1, 2013

Primary Completion (Anticipated)

August 1, 2013

Study Completion (Anticipated)

August 1, 2013

Study Registration Dates

First Submitted

July 18, 2013

First Submitted That Met QC Criteria

July 26, 2013

First Posted (Estimate)

July 29, 2013

Study Record Updates

Last Update Posted (Estimate)

July 29, 2013

Last Update Submitted That Met QC Criteria

July 26, 2013

Last Verified

July 1, 2013

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Circumcicsion

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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