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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03761862
Other study ID # Neuraltherapyinbtl
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2016
Est. completion date December 1, 2018

Study information

Verified date November 2018
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 was to explore the effect of neural therapy on postoperative pain and discomfort such as abdominal swelling; and gynecologic symptoms such as dysmenorrhea, dyspareunia, amount of menstrual bleeding and vaginitis. It also aimed to find out any possible links between the clinical changes and pathophysiologic mechanisms. One hundred and thirteen patients were randomly divided into two groups (neural therapy and control). Postoperative first day, neural therapy was applied to the T10 to S4 dermatomes and utero-vaginal ganglion in random with local anesthetic agent. All patients were recalled one year after the treatment. The visual analog scale (VAS) were noted in both groups, also discomfort and gynecologic symptoms are recorded.


Recruitment information / eligibility

Status Completed
Enrollment 113
Est. completion date December 1, 2018
Est. primary completion date December 1, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients who undergo bilateral tubal ligation

Exclusion Criteria:

- Previous abdominal surgery

- Patients with diseases that could have neurologic complications (DM, SLE ...)

Study Design


Intervention

Procedure:
Neural Therapy
Neural therapy is a form of alternative medicine in which local anesthetic is injected into certain locations of the body in an attempt to treat chronic pain and illness.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Kanuni Sultan Suleyman Training and Research Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Pain scores Visual Analog Scale was used as the pain scale.1 to 10 points are given here. High score (8- 10) indicates severe pain. 1 year later
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