Study of Intravenous Dexamethasone to Extend Spinal Anesthesia Duration in Pregnant Women Undergoing Cesarean Section
Led by Rawalpindi Medical College · Updated on 2025-07-28
110
Participants Needed
1
Research Sites
N/A
Total Duration
AI-Summary
What this Trial Is About
Lower segment cesarean section is a common surgery performed worldwide, usually under spinal anesthesia. This anesthesia involves injecting a local anesthetic near the spinal cord to block nerve signals, providing pain relief during and shortly after surgery while avoiding drug exposure to the baby. The study evaluates whether adding the steroid drug dexamethasone can prolong the duration of this spinal anesthesia and pain relief for pregnant patients during cesarean sections.
The study compares two groups one receiving 8 mg of dexamethasone intravenously immediately after the spinal anesthesia, and the other receiving a placebo of normal saline. This drug is known for its anti-inflammatory and anti-nausea effects and is being assessed here as an add-on to potentially extend anesthesia duration and post-operative pain relief. The trial is randomized and double-blind, meaning neither patients nor researchers know which treatment is given.
Participants will be monitored for how long the spinal block lasts after surgery, specifically measuring the time until the anesthesia effect decreases by two dermatomes. Researchers will also track the time until participants request additional pain medication. Safety, pain levels, and other outcomes will be assessed during and after the procedure. The study includes women aged 16 to 40 undergoing elective cesarean sections under spinal anesthesia and will follow them through the surgical and recovery periods.
CONDITIONS
Brief Title
Dexamethasone in Prolonging the Duration of Spinal Anesthesia Among Pregnant Patients
Research Team
H
Huda Tariq, MBBS
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American Society of Anesthesiologists (ASA) class II or higher
Scheduled for elective cesarean section under spinal anesthesia
You will not qualify if you...
Diagnosis of gestational diabetes
Body mass index greater than 35 kg/m2
Diagnosis of diabetes mellitus
Adrenal insufficiency
Chronic steroid use
Allergy to study medications
Sensory block level below T4
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Treatment
Duration - Until end of cesarean section and immediate post-operative period
Participants receive spinal anesthesia for elective cesarean section and are administered either intravenous Dexamethasone or placebo immediately after the sub-arachnoid block to prolong anesthesia duration.
1 treatment visit (in-person)
Post-operative Follow-up
Duration - Post-operative period (minutes to hours after surgery)
Participants are monitored for the duration of block regression and time to rescue analgesia after surgery.
1 follow-up visit (in-person)
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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Published Research Related To This Trial
Effect of intravenous dexamethasone on the duration of hyperbaric bupivacaine spinal anesthesia in lower abdominal surgery, Randomized controlled trial.
Amani H Abdel-Wahab, Essam S Abd Alla, Taghreed Abd El-Azeem