Status:
COMPLETED
A Trial for Peroperative Procedure and Postoperative Pain After Rectal Misoprostol or Rectal Hyoscine Administration
Lead Sponsor:
Bezmialem Vakif University
Conditions:
Hysteroscopic Surgery
Pain, Postoperative
Eligibility:
FEMALE
18-55 years
Phase:
NA
Brief Summary
Dilatation of the cervix is necessary before operative hysteroscopic procedures. This dilatation with Hegar dilators has certain difficulties and is associated with pain. Cervical priming with various...
Detailed Description
The study is planned as a double blind randomised controlled one centre study. It will take part at a operative gynaecological department of a university hospital. Women who apply to the university cl...
Eligibility Criteria
Inclusion
- Reproductive aged women
- Women who are scheduled for hysteroscopy for indications of endometrial polyp, submucous myoma or synaechiae
Exclusion
- Women who have undergone hysteroscopy previously
- women who are in menopause
Key Trial Info
Start Date :
June 11 2018
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 13 2018
Estimated Enrollment :
120 Patients enrolled
Trial Details
Trial ID
NCT03359655
Start Date
June 11 2018
End Date
December 13 2018
Last Update
December 27 2018
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
Bezmialem Vakif University
Istanbul, Turkey (Türkiye), 34093