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EFFECT OF LOW DOSE DEXAMETHASONE, ON BLOOD SUGAR CHANGES, IN DIABETIC AND NON-DIABETIC PATIENTS UNDERGOING ELECTIVE LOWER ABDOMEN AND LOWER LIMB SURGERIES

EVALUATION OF PERIOPERATIVE HYPERGLYCAEMIC RESPONSE TO ANTI-EMETIC DOSE OF DEXAMETHASONE, IN DIABETIC AND NON-DIABETIC PATIENTS UNDERGOING ELECTIVE LOWER ABDOMEN AND LOWER LIMB SURGERIES: A PROSPECTIVE, OBSERVATIONAL STUDY

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2020/06/025765
Enrollment
80
Registered
2020-06-09
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: K460- Unspecified abdominal hernia withobstruction, without gangrene Health Condition 2: S729- Unspecified fracture of femur Health Condition 3: S829- Unspecified fracture of lower leg

Interventions

Intervention1: Inj Dexamethasone 8mg IV stat at time of premedication before spinal anaesthesia: Inj Dexamethasone 8mg IV stat at time of premedication before spinal anaesthesia

Sponsors

Kamal Nayan Joshi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) ASA Grade I & II 2) Superficial lower abdominal or lower limb surgery. 3) Surgeries planned under subarachnoid block 4) Patients with controlled blood sugar levels (FBS 5) Age between 30 years - 60 years. 6) Body mass index 7) Surgery lasting for 1-2 hours. 8) Hospital stay; for at least 48 hours.

Exclusion criteria

Exclusion criteria: 1) Patientâ??s refusal. 2) ASA Grade III & IV. 3) Surgeries planned under general anaesthesia. 4) Diabetic patients with blood sugar levels (FBS >130mg/dl). 5) Patients with bleeding diathesis. 6) Patients with electrolyte imbalances. 7) Patients with cardio-respiratory disease. 8) Patients with hepatorenal disease. 9) Patients allergic to the study drug or local anaesthetic. 10) Patients with history of treatment with steroids in last 3 months. 11) Any neuro-psychiatric illness. 12) Pregnancy 13) Obesity (body mass index >30 Kg/m2). 14) Day care surgeries.

Design outcomes

Primary

MeasureTime frame
1. To assess the perioperative blood sugar level changes in diabetic and non-diabetics after administration of single dose dexamethasoneTimepoint: 1. To assess the perioperative blood sugar level changes in diabetic and non-diabetics after administration of single dose dexamethasone

Secondary

MeasureTime frame
1. To assess the time of onset for hyperglycemia in diabetic and non diabetics (if it is there). 2. To assess the requirement of insulin & dextrose containing fluid. 3. To assess the hemodynamic parameter changes e.g. heart rate, non-invasive blood pressure, oxygen saturation, and electrocardiogram. 4. To assess for any adverse outcome during study period. Timepoint: Blood sugar levels will be measured hourly up to 3 hours from T0(time of injection dexamethasone) and labelled T1, T2 and T3; then 6 hourly from T0 till next 24 hours and 12 hourly for next 24 hours.

Countries

India

Contacts

Public ContactDr Urmila Palaria

Government Medical College, Haldwani

urmila_palaria@rediffmail.com9897088443

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 9, 2026