Comparison of the additive effect of dexmedetomidine and neostigmine to bupivacaine on pain intensity after cesarean section with spinal anesthesia

Phase 2

• Conditions: Other acute postprocedural pain.; Other acute postprocedural pain; G89.18

• Registration Number: IRCT20161126031095N2
• Lead Sponsor: Mazandaran University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 30 August 2021

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 110

Inclusion Criteria

Women who have had a cesarean delivery

Exclusion Criteria

Patients who have refused to participate
Drug addiction
Have underlying diseases (moderate or severe heart, kidney, lung or nerve disease, significant scoliosis, kyphosis, obesity or blood clotting disease)
Patients with a height of less than 130 cm or aBody mass Index ( BMI) of more than 35

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain after cesarean section. Timepoint: Hours 0, 2, 4, 8 and 12. Method of measurement: According to the Visual Analogue Scale criteria.

Secondary Outcome Measures

Name	Time	Method
Sedation. Timepoint: 0,2,4,8,12. Method of measurement: Ramsay Criteria.;Immobilization. Timepoint: 0,2,4,8,12. Method of measurement: Bromage scale.;Moderate arterial blood pressure. Timepoint: 0,2,4,8,12. Method of measurement: Checklist.;Oxygen saturation. Timepoint: 0,2,4,8,12. Method of measurement: pulse oximetry.;Apgar score. Timepoint: 0,2,4,8,12. Method of measurement: Checklist.