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TO COMPARE THE EFFECTS OF SPLIT DOSE OF DEXAMETHASONE GIVEN PREOPERATIVELY AND POSTOPERATIVELY VERSUS SINGLE DOSE OF DEXAMETHASONE GIVEN PREOPERATIVELY ON POSTOPERATIVE NAUSEA AND VOMITING IN PATIENTS POSTED FOR LAPAROSCOPIC GYNAECOLOGIACAL SURGERIES LASTING 2-3 HOURS

Comparison of perioperative Dexamethasone split between two doses versus preoperative single dose for postoperative nausea and vomiting in Laparoscopic Gynecological Surgeries: A prospective randomized double-blind trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/101554
Enrollment
130
Registered
2026-01-19
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Health Condition 1: - Health Condition 2: N998- Other intraoperative and postprocedural complications and disorders of genitourinary system

Interventions

Intervention1: ADMINISTERATION OF 4MG DEXAMETHASONE BEFORE INDUCTION: 65 PATIENTS WILL RECEIVE 4MG BOLUS DOSE OF DEXAMETHASONE AT THE TIME OF INDUCTION Control Intervention1: SPLIT DOSE OF DEXAMETHASO

Sponsors

Dr Ananta Srilalita Bulusu
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA CLASS 1 AND 2

Exclusion criteria

Exclusion criteria: 1.PATIENTS WHO REFUSE TO GIVE CONSENT 2.PATIENTS WHO HAVE HISTORY OF ALLERGY TO DEXAMETHASONE 3.PREGNANT PATIENTS 4.PATIENTS WITH DIABETES MELLITUS 5.RHEUMATOID IMMUNE SYSTEM DISEASES 6.LIVER AND KIDNEY FAILURE

Design outcomes

Primary

MeasureTime frame
TO COMPARE THE EFFECTS OF SPLIT DOSE OF DEXAMETHASONE GIVEN PREOPERATIVELY AND POSTOPERATIVELY VERSUS SINGLE DOSE OF DEXAMETHASONE GIVEN PREOPERATIVELY ON POSTOPERATIVE NAUSEA AND VOMITING IN PATIENTS POSTED FOR LAPAROSCOPIC GYNAECOLOGIACAL SURGERIES LASTING 2-3 HOURSTimepoint: TO ASSESS POSTOPERATIVE NAUSEA VOMITING AT 0, 6, 12, 18, 24, 48, 72 HOURS—

Secondary

MeasureTime frame
effect of dexamethasone on blood sugar levelsTimepoint: 24 hours after the surgery—

Countries

India

Contacts

Public ContactAnanta Srilalita Bulusu

Karnataka medical college and research institute

ashvenki.hubli@gmail.com7348841250

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026