Rectointercostal nerve block both side of upper abdomen in adult patients for pain management

Analgesic efficacy of ultrasound guided bilateral recto-intercostal fascial plane block in adult patients undergoing upper midline incision abdominal surgery: A randomised control trial - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/10/075246

Enrollment

Registered

2024-10-14

Start date

Unknown

Completion date

Unknown

Last updated

2024-11-11

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Group I : Bilateral recto intercostal fascial plane block: Group I: will receive a bilateral recto intercostal fascial plane block after general anesthesia with IV PCA analgesia. bupiva

Eligibility

Inclusion criteria

Inclusion criteria: 1.ASA I/II 2.Age (Either Sex) – 18 to 70 years 3.Scheduled for upper midline incision abdominal surgery

Exclusion criteria

Exclusion criteria: 1.Mental disorder 2.Communication failure 3.Inability to understand the functionality of patient-controlled analgesia pump

Design outcomes

Primary

Measure	Time frame
To measure Post-operative morphine consumptions in 24 hours.Timepoint: To measure Post-operative morphine consumptions in 24 hours.	—

Secondary

Measure	Time frame
1) Intraoperative fentanyl consumption 2) Time of first rescue analgesia 3) Postoperative Pain Score (NRS) at 30 min, 2hour, 4 hour, 8 hour, 12 hour, 24 hour. 4) Adverse effect Timepoint: 24 hours	—

Countries

India

Contacts

Public ContactPoonam Kumari

All India Institute of Medical Sciences,Patna

drpoonam1981@gmail.com9473199126

Outcome results

None listed

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