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Comparison of Analgesic Efficacy in Video-Assisted Thoracoscopic Surgery Patients

NCT06352398 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 52

Last updated 2024-04-08

No results posted yet for this study

Summary

The 52 patients included in the study were divided into two groups as ESPB (n=26) and SPSIPB (n=26). Before the operation, 0.25% bupivacaine 30 ml was administered to both groups. After admission to the operating room, all patients underwent standard anaesthesia procedures. Morphine 0.05 mg/kg i.v. and parol 1 g i.v. were administered 30 min before the end of the operation. Post operatively the patient was followed up with controlled analgesia. Demographic data, ASA scores, body mass indexes, peri-operative haemodynamic values, remifentanil consumption and duration of surgery were recorded. Post-operative first 24 hours NRS scores, morphine consumption, number of nausea and vomiting episodes were recorded.

Conditions

  • Video-Assisted Thoracoscopic Surgery

Interventions

PROCEDURE

erector spina plan block

erector spina plan block

PROCEDURE

Serratus posterior superior intercostal plan block (SPSIPB)

Serratus posterior superior intercostal plan block (SPSIPB)

DRUG

0.25% bupivacaine

Before the operation, 0.25% bupivacaine 30 ml was administered to both groups.

Sponsors & Collaborators

  • Burcu Bozdogan Tuysuz

    lead OTHER

Principal Investigators

  • burcu bozdogan tuysuz · medenıyet unıversıty

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-12-20
Primary Completion
2024-02-01
Completion
2024-04-01

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06352398 on ClinicalTrials.gov