Not Yet RecruitingPhase 4ketamine

Comparison Between Ketamine Intrathecal and iv Dexamethasone for Post Cesarean Analgesia

Sponsored by Assiut University

NCT ID
NCT06408974
Target Enrollment
90 participants
Start Date
2024-12-01
Est. Completion
2024-12-20

About This Study

The aim of our study is to compare the postoperative analgesic efficacy of intrathecal ketamine added to bupivacaine to that of intravenous dexamethasone in patients undergoing cesarean section under bupivacaine spinal anesthesia.

Conditions Studied

Post Cesarean Analgesia

Interventions

  • Ketamine
  • dexamethasone

Eligibility

Sex:FEMALE
Age:18 Years - 45 Years
Healthy Volunteers:Yes
View full eligibility criteria
Inclusion Criteria:

* Age between 18 and 45 years
* Body mass index (BMI) of 18-35 kg/m2
* Patients with the American Society of Anesthesiologists (ASA) physical status I/II,
* Patients scheduled for elective cesarean section .
* females. .

Exclusion Criteria:

* Patient refusal
* Allergy to local anaesthetics
* Infection at the site of injection
* Coagulopathy,
* Chronic pain syndromes
* Prolonged opioid medication
* Patients who received any analgesic 24 h before surgery

Interested in this trial?

Contact the study team to learn more about eligibility and enrollment.

rokaya ma khalifa, resident
CONTACT
01013940535Rokayakhalifa495@gmail.com
mostafa sa abbas, dr
CONTACT
01003060187mostafasamy@aun.edu.eg
View on ClinicalTrials.gov
Data Source
ClinicalTrials.gov

Last updated from source