A clinical trial to study the effects of two drugs to compare efficacy and safety between Diclofenac Sodium and Tramadol in post Cesarean delivery pain relief in patients of Preeclampsia
Phase 3
- Conditions
- Health Condition 1: null- Analgesia in post LSCS patients with preeclampsia with routinely used analgesics (Tramadol - Opiod and Diclofenac - NSAID)
- Registration Number
- CTRI/2013/02/003395
- Lead Sponsor
- Dr Borade Sanjio Bhimraoji
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 200
Inclusion Criteria
Post LSCS patients with PE from PNC ward of Gynecology and Obstetrics Deptt ready to give informed consent.
Exclusion Criteria
1.Patient with Eclampsia.
2.Patient with PE with Renal Failure.
3.Patient with PE with Cardiac decompensation.
4.Normotensive patients who underwent LSCS for other obstetric indications other than PE.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method i) Efficacy and safety of Tramadol in post LSCS analgesia in Preeclampsia. <br/ ><br>ii) Efficacy and safety of Diclofenac Sodium in post LSCS analgesia in Preeclampsia. <br/ ><br>Timepoint: for 8 days during indoor period <br/ ><br>
- Secondary Outcome Measures
Name Time Method i) Comparative study between these two for Efficacy and safety.Timepoint: for 8 days during indoor period