FindTrial
Sign In

compare the effect on quality of recovery between epidural and erector spine plane block after surgery for lung cancer

Comparison of impact of erector spinae plane block versus thoracic epidural analgesia on perioperative quality of recovery in onco-surgical patients undergoing unilateral thoracotomy: a prospective, randomized control, open-label, non-inferiority, preliminary trial (CEPET Trial) - CEPET TRIAL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/05/052318
Enrollment
60
Registered
2023-05-04
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: C348- Malignant neoplasm of overlappingsites of bronchus and lung

Interventions

Intervention1: Ultra sound guided Erector spinae plane block (US ESPB): Unilateral ultra-sound guided ESPB (US-ESPB) at T5 or T6 level will be performed and catheter will be inserted. Study drugs will

Sponsors

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients of 18-65 years of age of either gender 2. American Society of Anaesthetist Physical Status I-II 3. Patients undergoing elective pneumonectomy, lobectomy or bilobectomy

Exclusion criteria

Exclusion criteria: 1. Refusal of consent 2. Patients already consuming morphine or fentanyl for analgesia 3. Contraindications of neuraxial anaesthesia 4. Renal or liver failure inhibiting the systematic use of paracetamol and/ or NSAIDs 6. Sensitivity to either of the trial drugs 7. Cognitive impairment 8. Not able to understand numerical rating pain scale (NRS) or QoR-15 questionnaire

Design outcomes

Primary

MeasureTime frame
Quality of recovery-15 (QoR-15) scoreTimepoint: On post operative day 1 (H24)—

Secondary

MeasureTime frame
Quality of recovery-15 (QoR-15) scoreTimepoint: on post operative day 2 (H48) and on discharge;NRS scoreTimepoint: H0, H24, H48 and on discharge;PFT (FEV1, FVC, FEV1/FVC)Timepoint: Preoperatively and H24;total fentanyl consumptionTimepoint: till discharge—

Countries

India

Contacts

Public ContactDr Surjyendu Ghosh

NCI, Jhajjar, AIIMS, NEW DELHI

dr.shwetabhopale06@gmail.com8178188976

Outcome results

None listed

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