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Comparison between two techniques of post operative pain relief in adult patients undergoing upper abdominal operation

Thoracic epidural analgesia(TEA) versus ultrasound guided transversus abdominis plane(TAP) block for postoperative pain relief in patients undergoing upper abdominal surgeries: A randomized controlled single blind comparative study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/02/079958
Enrollment
80
Registered
2025-02-04
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Thoracic Epidural Analgesia: To determine the post operative pain relief by Post operative numeric pain rating scores according to VAS assessed at specified time e.g. just after extubat

Sponsors

Department of Anaesthesiology IPGME&R,Kolkata
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.ASA physical status I,II,III 2.Age 20yrs to 60 yrs 3.Any gender 4.Dermatomal level of surgical incision and drain sites: a)upper abdominal surgical incisions where the lower end was at or above the thoracic T10 dermatome will be be included. b)The incisions included extended subcostal incision, transverse incision, chevron (rooftop) incision up to anterior axillary line.

Exclusion criteria

Exclusion criteria: 1.Excluded patients with a history of relevant drug allergy or chronic pain. 2.Lower end of the incision extended below T10 or extended laterally beyond the anterior axillary line. 3.Patient with cardiac, renal,hepatic,respiratory,coagulation dysfunction. 4.Age less than 20 years and more than 60 years of age. 5.Patient having infection at the site of procedure ,psychological disorder. 6.Patient with chronic use of pain medication. 7.Patient having BMI more than 30. 8.Non consenting patients. 9.History of previous surgery in the same dermatomal level.

Design outcomes

Primary

MeasureTime frame
Pain scores : Numeric pain rating scores according to VAS assessed at specified time points postoperatively.In case of breakthrough pain or demand dose of rescue analgesic, the particular time point and VAS score will be noted separately.Timepoint: Just after extubation, every one hourly for first 4 hr, every 2 hourly for 6 hrs, then 4 hourly till 24 hrs, then 12 hourly till first 72 hours

Secondary

MeasureTime frame
1.Opioid consumption : Total consumption(injection Fentanyl 50 mcg iv bolus as rescue analgesic) within first 24 hours post surgery. 2.Haemodynamic variables assessed at specified time points postoperatively. 3.Incidence of adverse events :Any complications or adverse reactions related to the anaesthesia technique or surgery(e.g. hypotension ,bradycardia, respiratory depression, local anaesthetic toxicity, hematoma). 4.Patient reported satisfaction scores:Subjective assessment of overall satisfaction with postoperative pain management using a standardised satisfaction questionnaire(e.g.Likert scale).Timepoint: just after extubation ,every one hourly for first 4 hr, every 2 hourly for 6 hr, then 4 hourly till 24 hrs, then 12 hourly till 1st 72 hours.

Countries

India

Contacts

Public ContactDR TAPAS GHOSE

Institute of Post Graduate Medical Education and Research

g.tapas@gmail.com9903745071

Outcome results

None listed

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