A clinical trial to compare the efficacy of pain and comfort scores for pain assessment
Not Applicable
Completed
- Conditions
- Health Condition 1: null- post caesarean section womenHealth Condition 2: O00-O9A- Pregnancy, childbirth and the puerperium
- Registration Number
- CTRI/2017/03/008248
- Lead Sponsor
- Dayanand Medical College and Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 180
Inclusion Criteria
All women who underwent caesarean section.
Exclusion Criteria
1.Age less than 18 years
2.Deaf and dumb patients
3.Patients with intellectual disability
4.History of chronic pain or opiate abuse
Study & Design
- Study Type
- Observational
- 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 pain perception in post-caesarean section women?
How do pain vs comfort scores compare to standard-of-care assessments for postpartum pain management?
Are there specific biomarkers that correlate with post-caesarean pain response variability?
What adverse events are commonly associated with postpartum pain management strategies and how are they managed?
What combination therapies or alternative approaches show promise in improving post-caesarean pain assessment and management?