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ESP VERSUS INTERCOSTAL NERVE BLOCK FOR PAIN IN RIB FRACTURES

INTERCOSTAL NERVE BLOCK (INB) VERSUS ERECTOR SPINAE BLOCK (ESP) FOR ANALGESIC EFFICACY IN PATIENTS WITH TRAUMATIC MULTIPLE RIB FRACTURES

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230822059225N1
Enrollment
380
Registered
2023-08-26
Start date
2023-04-01
Completion date
Unknown
Last updated
2023-10-16

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

Conditions

Rib fracture. Multiple fractures of ribs

Interventions

Intervention 1: Intervention group: Group E: Erector spinae block group.Patients in Group E received intravenous 0.5% bupivacaine with 2% lignocaine diluted in distilled water to make a total volume o

Sponsors

CMH Gujranwala
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 55 Years

Inclusion criteria

Inclusion criteria: Included all male and female patients between ages 25-55 years presenting in the operating room for pain relief with regional block with multiple rib fractures (>2 ribs) Not requiring surgical intervention for repair Under observation in the high dependency unit

Exclusion criteria

Exclusion criteria: Patients with metastatic disease Major cardiac or respiratory disease, low ejection fraction or post chemotherapy Allergy to lignocaine or bupivacaine Patients with advanced polytrauma causing hemodynamic instability Patients with oxygen saturation less than 92% after supplemental oxygen Patients with flail chest or pneumothorax Patients unwilling to be included in the study

Design outcomes

Primary

MeasureTime frame
Time to first dose of rescue analgesia. Timepoint: 24 hours after intervention. Method of measurement: Pain score above 5 on the standard visual analog scale.;Total dose of analgesia given. Timepoint: In 24 hours after intervention. Method of measurement: Dose charting of intravenous nalbuphine once pain scores above 5 after intervention.;Patient satisfaction. Timepoint: 24 hours after intervention. Method of measurement: Standard 7 point Likert scale.

Secondary

MeasureTime frame
Nausea/Vomiting. Timepoint: In 24 hours after intervention. Method of measurement: Frequency of episodes by the resident anesthetist on duty in HDU.;Hypotension. Timepoint: In 24 hours after intervention. Method of measurement: Systolic BP <80 and Diastolic <60 mmHg monitored and charted hourly.;Post-procedure sedation. Timepoint: In 24 hours after intervention. Method of measurement: Digital sphygmomanometer.

Countries

Pakistan

Contacts

Public ContactTaimur Afridi

Combined Military Hospital Gujranwala

taimurazamafridi@yahoo.com+92 346 5051728

Outcome results

None listed

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