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NCT04747171 Clinical Trial

Intrathecal Additives for Spinal Anaesthesia in Elective Caesarean Sections

Pain, Postoperative Clinical Trial

Official title:
A Comparative Study of Postoperative Analgesia of Different Intrathecal Additives for Spinal Anaesthesia in Elective Caesarean Sections

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT04747171
Other study ID # spinal additives
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date April 2021
Est. completion date July 2021

Study information
Verified date February 2021
Source Benha University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

we designed this randomized, single -blind, prospective clinical study to test postoperative analgesia of three intrathecal additives in elective caesarean sections which are magnesium, dexamethasone and dexmedetomidine.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 105
Est. completion date July 2021
Est. primary completion date June 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria: - American Society of Anesthesiologists classII-III adult female patient (age :18 -40 years old ) - Elective cesarean section under spinal anaesthesia - Gestational age > 37 weeks - BMI less than 30 kg/m2 Exclusion Criteria: - Patient refusal - unable to give consent - age < 18 or > 40 - BMI more than 30 kg/m2 - known allergy to the study medication - coagulopathies or on anticoagulant medications - diabetic neuropathy - patients with psychiatric disorders

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• intrathecal Magnesium
intrathecal adjuvants to bupivacaine
• intrathecal dexamthasone
intrathecal adjuvants to bupivacaine
• intrathecal dexmedetomidine
intrathecal adjuvants to bupivacaine

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Benha University

Outcome
Type Measure Description Time frame Safety issue
Primary analgesic effect duration of sensory block Up to 24 hours after surgery
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