Actively Recruiting

Phase 4
Age: 16Years - 40Years
FEMALE
Healthy Volunteers
ID07088146

Role of Intravenous Dexamethasone in Prolonging the Duration of Spinal Anesthesia in Pregnant Patients Undergoing Lower Segment Cesarean Section

Led by Rawalpindi Medical College · Updated on 2025-07-28

110

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

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

Who Can Participate

Age: 16Years - 40Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Female patients aged between 16 and 40 years
  • American Society of Anesthesiologists (ASA) class II or higher
  • Scheduled for elective cesarean section under spinal anesthesia
Not Eligible

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

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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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)

Trial Site Locations

Total: 1 location

1

Benazir Bhutto Hospital Rawalpindi

Rawalpindi, Punjab Province, Pakistan, 46000

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Research Team

H

Huda Tariq, MBBS

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

https://pubmed.ncbi.nlm.nih.gov/37736711