Investigating the effect of ultrasound- guided bilateral dual TAP block and erector spine plane block
Phase 3
- Conditions
- Pain.Pain
- Registration Number
- IRCT20230424057986N2
- Lead Sponsor
- Iran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Female
- Target Recruitment
- 60
Inclusion Criteria
Women with uterine diseases and candidates for full abdominal hysterectomy
Age between 20-60 years
A person with normal health
A person with mild systemic disease
Exclusion Criteria
Allergy to any of the drugs used in the study
Addiction to alcohol, benzodiazepines and narcotics
The presence of underlying diseases including kidney disease, liver disease, heart failure, arrhythmia or valvular heart disease.
Coagulation disorder
Contraindications for regional anesthesia
Emergency patients
Patients who have received analgesics in the last 24 hours
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Severity of patients' pain. Timepoint: 1, 2, 4, 8, 12 and 24 hours after surgery. Method of measurement: Based on visual analog scale.
- Secondary Outcome Measures
Name Time Method