Skip to content

To assess the efficacy and applicability of a single injection of Erector spinae plane in video assisted thoracoscopic surgeries

A single-arm prospective interventional study to assess the feasibility and efficacy of single-shot Erector spinae block in patients undergoing video-assisted lung resection surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/05/019413
Enrollment
25
Registered
2019-05-29
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: C349- Malignant neoplasm of unspecifiedpart of bronchus or lung

Interventions

Intervention1: Erector Spinae Plane Block: Ultrasound guided Erector spinae plane block is given to block the dermatomes from T3 to T8. The block is given immediately after the end of surgery, only on

Sponsors

TATA MEMORIAL CENTRE
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient posted for VATS procedure for unilateral pulmonary metastatectomy Patients who are not planned for thoracic epidural analgesia BMI 19-30 kg/m2 ASA I, II & III Age group: 18-75 years

Exclusion criteria

Exclusion criteria: Local site infection. Refusal of consent. Allergy to local anaesthetic Coagulopathy defined as platelet counts less than 75000/mm3 or INR > 1.4. On chronic pain medication for more than 1 week in the 4 weeks preceding surgery.

Design outcomes

Primary

MeasureTime frame
Feasibility To assess presence of unilateral band of hypoalgesia on the operative side and check for the dermatomes covered by the block over the anterior chest wall and compare it with the sensations on the non-operative side. This will be elicitedin the PACU by 1 member of APS team and 1 independent memberTimepoint: 2 hours of shifting to PACU, and thereafter at 4hr, 6hr, 12hrs and 24 hrs.

Secondary

MeasureTime frame
Pain scores (at rest & cough) Percentage of patients receiving Rescue analgesics or PCA pumpsTimepoint: 2hr, 4hr, 6hr, 12hr and 24hrs interval

Countries

India

Contacts

Public ContactDr DHANASHRI KARKHANIS

Tata Memorial Centre

ragstho24@rediffmail.com9769077764

Outcome results

None listed

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