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Effect of Dexamethasone on pain relief after cesarean section

COMPARISON OF TWO DOSES OF INTRAVENOUS DEXAMETHASONE ALONG WITH SPINAL ANESTHESIA FOR POST OPERATIVE ANALGESIA IN LOWER SEGMENT CESAREAN SECTION - no

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/03/050863
Enrollment
66
Registered
2023-03-20
Start date
Unknown
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium

Interventions

Intervention1: Post-operative analgesic efficacy of intravenous dexamethasone: Post-operative analgesic efficacy of two doses of intravenous dexamethasone i.e. 4mg and 8mg at 0, 2, 4, 8, 12, 16 and 24

Sponsors

Shree Krishna hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients undergoing lower Segment caesarean section under spinal anaesthesia. 2.All patients with fasting period of 6 hours to solids and 2 hours to liquids 3.American Society of Anesthesiologists Physical Status grade II

Exclusion criteria

Exclusion criteria: 1.High risk pregnancy â?? Eclampsia, Preeclampsia, Abruption placenta, Placenta Previa, Cord prolapse, Pregnancy with medical disordered (Diabetes mellitus, Cardiac disease, Thyroid disease) 2.Multiple gestations 3.Caesarean with fetal distress 4.Absolute contraindication to spinal anaesthesia 5.Patients on steroid therapy or past history of medication with steroids in last 1 year 6.Diabetic patient with HbA1c of more than 8 7.Obese patient with BMI > 40 8.Intraoperative blood loss of more than 20% 9.Pre-operative hemoglobin level less than 8 mg/dl 10.Patients with Raised CRP and total leucocyte counts 11.Allergy to local anaesthetic drug 12.Severe spinal deformity

Design outcomes

Primary

MeasureTime frame
ï?¶To evaluate post-operative analgesic efficacy of two doses of intravenous dexamethasone i.e. 4mg and 8mg at 0, 2, 4, 8, 12, 16 and 24 hours by using numeric rating scale(NRS)Timepoint: After completion of Spinal anaesthesia till 24 hours

Secondary

MeasureTime frame
1.Duration of analgesia. 2.Incidence of nausea, vomiting intraoperative and post-operative 3.Incidence of shivering intraoperative and post-operative Timepoint: post-operative till 24 hours.

Countries

India

Contacts

Public ContactDr Parthkumar Kishankumar Sarvaiya

Shree Pramukhswami Medical College

dr.niralipanchal@gmail.com9825031808

Outcome results

None listed

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