Skip to content

comparison of serratus anterior plane block with erector spinae plane block for pain relief after video assisted thoracic surgery.

SERRATUS ANTERIOR PLANE BLOCK VERSUS ERECTOR SPINAE PLANE BLOCK FOR POSTOPERATIVE ANALGESIA IN VIDEO-ASSISTED THORACIC SURGERY - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/12/060584
Enrollment
40
Registered
2023-12-20
Start date
Unknown
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Health Condition 1: J418- Mixed simple and mucopurulent chronic bronchitis Health Condition 2: J869- Pyothorax without fistula

Interventions

Intervention1: Serratus anterior plane block: Patient will be placed in lateral position with 90 degree abduction of upper arm. Ultrasound probe will be placed in mid clavicular region.of thoracic cag

Sponsors

Dayanand Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1Patient aged 18 - 65 years, who are competent to give informed consent. 2Either gender 3ASA I, II and III 4Patient posted for unilateral elective video assisted thoracic surgery under general anaesthesia

Exclusion criteria

Exclusion criteria: 1Infection at the site of block 2Coagulopathy 3Drug addicts or history of opioid dependence 4Pre-existing chronic pain or cognitive dysfunction 5History of allergy to opioids or local anaesthetics • Patient with severe liver, renal, cardiac disease and/or rhythm disorder. • Patient requiring post op mechanical ventilation • Patient receiving anticoagulation or any bleeding disorder • Patient refusal • Pregnancy

Design outcomes

Primary

MeasureTime frame
Time to need of first rescue opioid analgesic: Time to need of first rescue analgesic will be recorded as the time from arrival in PACU till the time of administration of first rescue opioid analgesic.Timepoint: Upto 72 hours postoperatively

Secondary

MeasureTime frame
1.NRS Pain score 2.Total 72 hours opioid consumption 3.Need for rescue opioid analgesic 4.Quality of patient recovery 5.Patient satisfaction 6.Side effectsTimepoint: 1.NRS Pain scores after 1,2,4,8,12,24,36,48,and 72 hours postoperatively 2.opioid consumption upto 72 hours 3.Need for rescue opioid analgesic upto 72 hours 4.Quality of patient recovery at 24 hours 5.Patient satisfaction at 72 hours 6.Side effects at 72 hours

Countries

India

Contacts

Public ContactPiyush Sharma

Dayanand Medical college and Hospital Ludhiana

sharmapiyush342@gmail.com8847290232

Outcome results

None listed

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