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Comparison of different doses of a combination of two drugs when injected in abdominal wall(rectus sheath) for post operative pain relief in surgeries requiring midline incision.

Comparative analgesic potency of ropivacaine0.2% versus 0.5% with dexmedetomidine as an adjuvant in preincision USG rectus sheath block for midline incision

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/08/009287
Enrollment
60
Registered
2017-08-08
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: null- Patient posted for emergency surgery for duodenal ulcer perforation.

Interventions

Intervention1: fff: fff Intervention2: Ropivacaine 0.25% (15 ml)with dexmedetomidine 1mcg per kg.: USG guided bilateral rectus sheath block with a total volume of 17ml on each side. Intervention3: Rop

Sponsors

Shalini Sharma
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)ASA 1 and 2 patients. 2)BMI 18.5-39.9. 3)Patients scheduled for emergency laparotomy for duodenal ulcer perforations.

Exclusion criteria

Exclusion criteria: 1)Patient refusal. 2)Bleeding and coagulation disorders. 3)Local infection at the block site. 4)Allergy to study drugs.

Design outcomes

Primary

MeasureTime frame
To compare the duration of post op analgesia after giving equal volumes and different concentration of ropivacaine 0.25% and 0.5% with dexmeditomidine 1mcg per kg in USG guided rectus sheath block.Timepoint: Every 30 min till pain starts.

Secondary

MeasureTime frame
Patient satisfaction with pain control. Number of a rescue analgesic requirement in 24 hours. Timepoint: After 24 hours.

Countries

India

Contacts

Public ContactShalini Sharma

Dr Rajendra Prasad Govt. Medical College Tanda at Kangra

shalini.medico@gmail.com9418011121

Outcome results

None listed

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