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Effect of single dose dexamethasone on variation in Blood Glucose level in pediatric hypospadias surgery: A Prospective Randomised controlled study in department of Anesthesia, SMS Medical college, Jaipur

A Randomized,controlled,Study for effect of single dose of intraoperative dexamethasone on variation in blood glucose level in pediatric hypospadias surgery in department of anesthesia,SMS Medical College,Jaipur - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/10/058560
Enrollment
72
Registered
2023-10-12
Start date
Unknown
Completion date
Unknown
Last updated
2023-10-16

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

Conditions

Health Condition 1: Q549- Hypospadias, unspecified

Interventions

Intervention1: single dose of intraoperative dexamethasone: Patients will be administered a single dose of I.V. dexamethasone (0.15mg/kg) intraoperatively and blood glucose will be monitored 2 hours p

Sponsors

Sawai Man Singh Medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Children (3-6 years) undergoing hypospadias surgery. Parents/caretaker willing to consent for participation. Patients belonging to American society of Anesthesiologists (ASA) grade I and II

Exclusion criteria

Exclusion criteria: Patients with Diabetes Mellitus. Patients on immunosuppressive /steroid therapy. Patients with known allergy to dexamethasone. Patients with hepatorenal dysfunction.

Design outcomes

Primary

MeasureTime frame
To evaluate & compare the difference, in change in blood glucose levels at various time points in dexamethasone v/s control group.Timepoint: Baseline(pre_operative), 2 hours after administration of dexamethasone/saline, Fasting blood sugar and Post prandial blood sugar on : Post_operative day: 1,2 and 3.

Secondary

MeasureTime frame
1. To assess & compare the difference in mean no of doses & total doses of rescue analgesic needed in post-operative period upto 12 hours in both the groups. 2. To assess & compare the difference in proportion of patients who experienced post-operative nausea, vomiting upto 12 hours in both the groups. 3. To assess & compare the percentage of patients who experienced side effects ( fever, surgical site infection) in both the groups.Timepoint: 1. To assess & compare the difference in mean no of doses & total dose of rescue analgesic needed in post-operative period upto 12 hours in both the groups. 2. To assess & compare the difference in proportion of patients who experienced post-operative nausea, vomiting, upto 12 hours in both the groups. 3. To assess & compare the percentage of patients who experienced side effects (fever, surgical site infection) in both the groups.

Countries

India

Contacts

Public ContactDr Isha Malhotra

SMS MEDICAL COLLEGE,JAIPUR

Neelam_dogra24@yahoo.com9928709289

Outcome results

None listed

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