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To see the effect of 0.375% Ropivacaine+ Dexamethasone and 0.25% LevoBupivacaine +Dexamethasone for Postoperative Analgesia after C-Section in USG guided Ilioinguinal-Iliohypogastric block:observational study in Pravara Rural hospital, Loni.

Effect of 0.375% Ropivacaine+ Dexamethasone and 0.25% LevoBupivacaine +Dexamethasone on Postoperative Analgesia after C-Section in USG guided Ilioinguinal-Iliohypogastric block - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/02/062676
Enrollment
260
Registered
2024-02-15
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Health Condition 1: O94- Sequelae of complication of pregnancy, childbirth, and the puerperium

Interventions

Intervention1: 0.375% Ropivacaine+ Dexamethasone and 0.25% LevoBupivacaine +Dexamethasone for Postoperative Analgesia after C-Section in USG guided Ilioinguinal-Iliohypogastric Block: To see the eff

Sponsors

Dr Balasaheb Vikhe Patil pravara rural medical college
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patient willing to give written, verbal, informed consent to participate in the study. 2.Patients undergoing lower segment caesarean section under spinal anaesthesia. 3.Belonging to ASA Class I OR II.

Exclusion criteria

Exclusion criteria: 1.Patients undergoing LSCS under general anaesthesia or in whom spinal anaesthesia was inadequate for the conduct of surgery 2.Patient having any systemic illness like hypertension, diabetes, thyroid or other endocrinologic illness, cardiovascular disease, coagulation disorders. 3.Patients who are unable to communicate and patient having psychiatric disorders.

Design outcomes

Primary

MeasureTime frame
To estimate the duration of postoperative analgesia from 1 hr till 24hrs after giving the blockTimepoint: To estimate the duration of postoperative analgesia from 1 hr to 24 hrs till after giving the block—

Secondary

MeasureTime frame
1.Total amount of rescue analgesia dose required in 1 day after surgery. 2.To study the quality of analgesia(visual analogue scale) in 24 hrs duration 3. To assess patient satisfaction score in 24hrs duration. 4. To study the variation in hemodynamic parameters {HR, BP, MAP, O2 saturation, RR}in 24hrs duration. 5.To assess the adverse effects (dry mouth, hypotension, severe vomiting)in 24hrs duration.Timepoint: 1.Total amount of rescue analgesia dose required in 1 day after surgery. 2.To study the quality of analgesia(visual analogue scale) till 1 day duration. 3.To assess patient satisfaction score in 1 day duration. 4.To study the variation in hemodynamic parameters {HR, BP, MAP, O2 saturation, RR} in 1 day duration 5.To assess the adverse effects (dry mouth, hypotension, severe vomiting) in 1 day duration—

Countries

India

Contacts

Public ContactChandana chowdary

Pravara institute of medical sciences,loni

tganesh55555@gmail.com9646284105

Outcome results

None listed

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