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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03891537
Other study ID # 2018.10.36
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2016
Est. completion date January 1, 2019

Study information

Verified date March 2019
Source Kanuni Sultan Suleyman Training and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this study is to evaluate the effect of nebulisation in patients with bilateral tubal ligation in the first postoperative year, the amount of dysmenorrhea, dyspareunia and menstrual bleeding, recurrent vaginitis and cystitis.

A retrospective analysis of bilateral tubal ligation with optional modified Pomeroy technique in the family planning unit and evaluation of the results of patients who underwent Neural Therapy during and postoperatively will be evaluated.


Recruitment information / eligibility

Status Completed
Enrollment 113
Est. completion date January 1, 2019
Est. primary completion date January 1, 2018
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- patients who underwent bilateral tubal ligation with modified Pomeroy technique,

- Patients with dysmenore, dyspareunia and menstrual bleeding,

Exclusion Criteria:

- postoperative asymptomatic

- Additional treatments for pain and complaints

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Turkey Kanuni Sultan Süleyman Training and Research Hospital Istanbul

Sponsors (1)

Lead Sponsor Collaborator
Kanuni Sultan Suleyman Training and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary postoperative dysmenorrhea Postoperative dysmenorrhea in the first postoperative year was evaluated by viscous pain scale (VAS) in patients who underwent bilateral tubal ligation with the modified Pomeroy technique. There is no pain at zero points according to visuel pain scale;Ten points are very severe - unbearable pain.
patients will score between one to ten pains.
1st year postoperative
Primary postoperative dyspareunia Postoperative dyspareunia in the first postoperative year was evaluated by viscous pain scale (VAS) in patients who underwent bilateral tubal ligation with the modified Pomeroy technique. There is no pain at zero points according to visuel pain scale;Ten points are very severe - unbearable pain.
patients will score between one to ten pains.
1st year postoperative
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