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role of dexamethasone and ondansetron as an adjunct in prevention of subarachnoid block related side effects in patients undergoing lower limb orthopedic surgeries

Comparison of effect of ondansetron as an adjuvant to dexamethasone on effects of subarachnoid block in patients undergoing lower limb orthopedic surgery :  a prospective randomized double blind controlled study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/08/056598
Enrollment
130
Registered
2023-08-17
Start date
Unknown
Completion date
Unknown
Last updated
2023-11-13

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

Conditions

Health Condition 1: M959- Acquired deformity of musculoskeletal system, unspecified

Interventions

Intervention1: dexamethasone group : In preoperative room, patients will receive dexamethasone 8mg diluted in 100cc NS i.v. (group D ) infusion over 15 minutes one hour prior to the induction Contr

Sponsors

Sir T general hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: a  prospective comparative randomized double blind controlled study, this randomized controlled clinical study will be carried out in patients in orthopedic operation theatre of sir T hospital ,government medical college , bhavnagar , Gujarat.

Exclusion criteria

Exclusion criteria: patient refusal, patients with anomalous spine ,patients with contraindication to spinal anesthesia eg coagulopathy , thrombocytopenia , allergy to local anesthetic and those on steroid or serotonin related medications

Design outcomes

Primary

MeasureTime frame
To compare the effect of intravenous administeration of dexamethasone and combination of dexamethasone with ondansetron on subarachnoid block induced hypotension ( primary outcome) in patients undergoing lower limb orthopedic surgeries Timepoint: at 0 min ( baseline just at induction) , 5 min , 10 min, 20 min, 30 min 60 min, 90 min , 120 min , 2.5 hours, 3 hours, 3.5 hours, 4 hours, 4.5 hours , 5 hours , 5.5 hours , 6 hours

Secondary

MeasureTime frame
post operative nausea vomitingTimepoint: 24 hrs

Countries

India

Contacts

Public ContactDR SOPHIYA ARORA

GOVERNMENT MEDICAL COLLEGE BHAVNAGAR GUJARAT

shah.komal212@gmail.com9877969725

Outcome results

None listed

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