Effectiveness of paracervical block for pain relief in women undergoing hysterosalpingography in Bayelsa State, South-South Nigeria: a randomized control trial
Not Applicable
Recruiting
- Conditions
- Fertility-female
- Registration Number
- PACTR202203697292254
- Lead Sponsor
- Authors
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 380
Inclusion Criteria
All women of reproductive age group between 15 and 49 years.
Women with primary or secondary infertility.
Exclusion Criteria
Patients that declined participation.
Allergy to dye.
Allergy to lignocaine.
Pelvic inflammatory disease.
Cyst on ultrasound scan.
Chronic pelvic pain
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie paracervical block efficacy in female fertility pain management?
How does paracervical block compare to standard analgesics for hysterosalpingography pain in Nigeria?
Are there specific biomarkers that predict optimal response to paracervical block in reproductive medicine?
What are the potential adverse events associated with paracervical block during hysterosalpingography procedures?
What combination therapies show enhanced pain relief for hysterosalpingography compared to paracervical block alone?