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Two Different Surgical Techniques on Postoperative Circumcision Pain

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ClinicalTrials.gov Identifier: NCT01909765
Recruitment Status : Unknown
Verified July 2013 by Reyhan Polat, Diskapi Yildirim Beyazit Education and Research Hospital.
Recruitment status was:  Not yet recruiting
First Posted : July 29, 2013
Last Update Posted : July 29, 2013
Sponsor:
Information provided by (Responsible Party):

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

Condition or disease Intervention/treatment Phase
Postoperative Pain Other: Dorsal slit Other: Double incision Phase 4

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

Study Design

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 30 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Triple (Participant, Investigator, Outcomes Assessor)
Official Title: Comparison of Two Different Circumcision Surgical Technique on Postoperative Pain
Study Start Date : July 2013
Estimated Primary Completion Date : August 2013
Estimated Study Completion Date : August 2013
Arms and Interventions

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 Name: Surgical technique


Outcome Measures

Primary Outcome Measures :
  1. To asses postoperative pain scores on Modified Objective Assessment Scale (MOAS) [ Time Frame: Postoperative first two hours ]

Eligibility Criteria

Information from the National Library of Medicine

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Ages Eligible for Study:   2 Years to 14 Years   (Child)
Sexes Eligible for Study:   Male
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Children

Exclusion Criteria:

  • Patients with any bleeding
Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): 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

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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
First Posted: July 29, 2013    Key Record Dates
Last Update Posted: July 29, 2013
Last Verified: July 2013

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

Additional relevant MeSH terms:
Pain, Postoperative
Pain
Neurologic Manifestations
Nervous System Diseases
Postoperative Complications
Pathologic Processes
Signs and Symptoms