Randomized Controlled Trial to Compare the Analgesic Efficacy and Safety of Paracervical Block and Conscious Sedation in the Surgical Evaluation of the Uterus Following First Trimester Incomplete Miscarriages
Not Applicable
- Conditions
- Anaesthesia
- Registration Number
- PACTR202108841661192
- Lead Sponsor
- SOPHIA NNENNA NWEKE
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Other
- Sex
- Female
- Target Recruitment
- 162
Inclusion Criteria
Incomplete miscarriage =13 weeks of gestation.
Stable patients
Exclusion Criteria
Patients with known history of allergy to the drugs.
Patients with infection at the site of the block.
Psychiatric or neurological diseases.
Presence of active pelvic inflammatory disease.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome measure was assessment of the efficacy of analgesia when paracervical<br>block was compared with conscious sedation, also for the requirement of supplementary<br>analgesia/anesthesia intraoperatively.
- Secondary Outcome Measures
Name Time Method The Secondary outcome measures were the incidence of complications, postoperative activity,<br>the feasibility of the procedure to be done for daycare and participant’s satisfaction. It also included<br>side effects of different agents in the surgical evacuation of incomplete miscarriage and maternal<br>satisfaction.