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Comparison of two types of pain relief methods (intrapleural block versus conventional analgesia) in alleviating pain and lung function in patients with chest drainage tube after trauma- a randomised controlled trial

Comparison of the effectiveness of intrapleural block versus conventional analgesia in pain relief and pulmonary function in patients with intercostal drainage for trauma- a randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/12/038507
Enrollment
57
Registered
2021-12-08
Start date
Unknown
Completion date
Unknown
Last updated
2022-02-21

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

Conditions

Health Condition 1: S272- Traumatic hemopneumothorax

Interventions

Intervention1: INTRAPLEURAL BLOCK: Patients receive 25cc of 0.25% bupivacaine Q8 hourly for 48 hours through the Intercostal Drain Tube plus 2ml normal saline slow iv and 100 ml normal saline iv bolus

Sponsors

Jawaharlal Institute of Postgraduate Medical Education and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All patients more than 18 years of age with intercostal drain for chest trauma

Exclusion criteria

Exclusion criteria: Patients with preexisting lung pathology Other preexisting chronic painful conditions (E.g. malignancy, chronic pancreatitis, etc.) Patients with GCS less than 15 Contraindications to intrapleural block â?? Allergy to local anaesthetic â?? Extensive block site infection â?? Emphysema â?? Bullous lung disease â?? Recent pleural disease or pleurodesis â?? Empyema â?? Coagulopathy Contralateral phrenic nerve palsy Patients not willing for incentive spirometry Patients requiring ventilatory support Hemodynamically unstable patients

Design outcomes

Primary

MeasureTime frame
PAIN RELIEF AS PER NUMERICAL RATING SCALE. 0 ON NRS FOR NO PAIN TO 10 FOR MAXIMUM POSSIBLE PAIN, AS REPORTED BY THE PARTICIPANT TO THE INVESTIGATORTimepoint: AT BASELINE; FOLLOWING PLACEMENT OF ICD; FOLLOWING ADMINISTRATION OF BLOCK; AND 8HOURLY FROM THEN FOR A PERIOD OF 48 HOURS (AT 8, 16, 24, 32, 40 AND 48 HOURS)

Secondary

MeasureTime frame
BREATH HOLDING TIME IN SECONDS, ASKING PATIENT TO HOLD BREATH AT FULL INSPIRATION FOR THE LONGEST DURATION POSSIBLE.Timepoint: BEFORE ICD PLACEMENT; FOLLOWING PLACEMENT OF ICD; FOLLOWING ADMINISTRATION OF BLOCK; AND 8HOURLY FROM THEN FOR A PERIOD OF 48 HOURS (AT 8, 16, 24, 32, 40 AND 48 HOURS);OTHER COMPLICATIONS LIKE PNEUMONIA, ARDS, WORSENING OF PNEUMOTHORAX.Timepoint: BEFORE ICD PLACEMENT; FOLLOWING PLACEMENT OF ICD; FOLLOWING ADMINISTRATION OF BLOCK; AND 8HOURLY FROM THEN FOR A PERIOD OF 48 HOURS (AT 8, 16, 24, 32, 40 AND 48 HOURS);PULMONARY FUNCTION IN TERMS OF MAXIMUM INSPIRATORY VOLUME AS MEASURED WITH INCENTIVE SPIROMETER IN mlTimepoint: BEFORE ICD PLACEMENT; FOLLOWING PLACEMENT OF ICD; FOLLOWING ADMINISTRATION OF BLOCK; AND 8HOURLY FROM THEN FOR A PERIOD OF 48 HOURS (AT 8, 16, 24, 32, 40 AND 48 HOURS);TIME TO FIRST ANALGESIA FROM THE TIME OF ADMINISTRATION OF DRUG THROUGH THE ICD, IN HOURS.Timepoint: BEFORE ICD PLACEMENT; FOLLOWING PLACEMENT OF ICD; FOLLOWING ADMINISTRATION OF BLOCK; AND 8HOURLY FROM THEN FOR A PERIOD OF 48 HOURS (AT 8, 16, 24, 32, 40 AND 48 HOURS)

Countries

India

Contacts

Public ContactMohammed Najeebuddin

JAWAHARLAL INSTITUTE OF POSTGRADUATE MEDICAL EDUCATION AND RESEARCH

elamurugantp@gmail.com9443648918

Outcome results

None listed

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