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NCT01909765 Clinical Trial

Two Different Surgical Techniques on Postoperative Circumcision Pain

Postoperative Pain Clinical Trial

Official title:
Comparison of Two Different Circumcision Surgical Technique on Postoperative Pain

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT01909765
Other study ID # Circumcicsion
Secondary ID
Status Not yet recruiting
Phase Phase 4
First received July 18, 2013
Last updated July 26, 2013
Start date July 2013
Est. completion date August 2013

Study information
Verified date July 2013
Source Diskapi Yildirim Beyazit Education and Research Hospital
Contact n/a
Is FDA regulated No
Health authority Turkey: Ministry of Health
Study type Interventional

Clinical Trial Summary

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

Description:

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

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 30
Est. completion date August 2013
Est. primary completion date August 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 2 Years to 14 Years
Eligibility Inclusion Criteria:

- Children

Exclusion Criteria:

- Patients with any bleeding

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor)

Related Conditions & MeSH terms

Intervention

Other:
• Dorsal slit
Skin and mucosa incision made together
• Double incision
Skin and mucosa incision made separately

Locations
Country Name City State
Turkey Diskapi Yildirim Beyazit Education and Research Hospital Ankara

Sponsors (1)
Lead Sponsor Collaborator
Diskapi Yildirim Beyazit Education and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary To asses postoperative pain scores on Modified Objective Assessment Scale (MOAS) Postoperative first two hours No
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