Comparison of efficacy of different modalities of ganglion impar block to relieve chronic pelvic pain in patients
Phase 1
- Conditions
- Health Condition 1: N949- Unspecified condition associated with female genital organs and menstrual cycle
- Registration Number
- CTRI/2020/10/028306
- Lead Sponsor
- Dr Madhav Verma
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Patient giving consent to participate in the study.
2. Female patients with chronic pelvic pain after ruling out any obstetrics and gyanecological cause through specialist opinion and USG or negative diagnostic laproscopy.
3. Patients above the age of 18 years and below 60 years
4. Patients who have had atleast two weeks trial of medications without significant effect.
5. Patient with normal anatomy for ganglion impar block.
Exclusion Criteria
1. Patients with bleeding disorders and the patients on anticoagulants.
2. Patients with uncontrolled systemic diseases.
3. Patients with infection or injury at the injection site.
4. Patients with coccygectomy.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method