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Comparison between two doses of the drug Dexamethasone on postoperative pain in patients undergoing caesarean section under spinal anaesthesia

Comparative evaluation of two doses of intravenous dexamethasone for postoperative analgesia in patients undergoing lower segment caesarean section under spinal anaesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/09/036984
Enrollment
70
Registered
2021-09-30
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Intravenous administration of Dexamethasone 4mg and Dexamethasone 8mg: Providing 4mg of Dexamethasone intravenously to pregnant women after delivery of baby by LSCS for postoperative an

Sponsors

Vardhman Mahavir Medical College and Safdarjung Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Pregnant females of age 18-40 years of American Society of Anaesthesiologists (ASA) physical status of class I and II undergoing lower segment caesarean section.

Exclusion criteria

Exclusion criteria: Patients with history of use of glucocorticoids 12hrs prior to the first planned dose and pre-existing dependence on narcotics or receiving chronic treatment with opioids and cortisol , history of drug allergy to dexamethasone or tramadol, history of Gestational Diabetes mellitus, Pregnancy induced hypertension, thyroid disorders, anaemia, asthma, heart failure, peptic ulcer and other high-risk pregnancies

Design outcomes

Primary

MeasureTime frame
Assessment of pain by Visual Analog Scale (VAS) scoreTimepoint: 0 hours(immediately after reaching postoperative care unit), 1hour, 2hours, 4hours, 6hours, 12hours, 18hours and 24hours after surgery.

Secondary

MeasureTime frame
Assessment of Adverse effectsTimepoint: Any adverse effects if present at any time will be noted and treated according to hospital protocol;Assessment of Blood SugarTimepoint: Blood sugar will be measured at the end of surgery, then at 6th hourly interval till 24hrs;Assessment of motor blockade graded by Modified Bromage scaleTimepoint: Every 30 minutes interval in postoperative period till complete recovery from spinal anaesthesia;Assessment of sensory blockade by Pin Prick for two segment regressionTimepoint: Every 30 minutes interval in postoperative period till complete recovery from spinal anaesthesia

Countries

India

Contacts

Public ContactDr Nikitha Vasan

Vardhman Mahavir Medical College and Safdarjung Hospital

drmeenakshi86@yahoo.com9899689829

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026