Comparison of Two Different Methods for Reducing Pain After Lung Surgery

NCT ID: NCT06260137

Last Updated: 2024-02-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-07-10

Study Completion Date

2024-08-31

Brief Summary

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The goal of this clinical study is to compare the effectiveness of the Rhomboid Intercostal Block and Sub-Servitus plan block and the effectiveness of the Rhomboid intercostal block in patients with video-supported thoracoscopic surgery. The main question it aims to answer is:

Which of these two blocks more effectively reduces the patients' pain?

Detailed Description

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Conditions

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Postoperative Analgesia

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

SINGLE

Participants

Study Groups

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Rhomboid İntercostal Block (RIB)

Group Type ACTIVE_COMPARATOR

Rhomboid intercostal block

Intervention Type PROCEDURE

Patients will be injected with a local anesthetic drug under the rhomboid intercostal muscle before surgery.

Rhomboid intercostal and subserratus plane block (RISS)

Group Type ACTIVE_COMPARATOR

Rhomboid intercostal and subserratus plane block

Intervention Type PROCEDURE

Patients will be injected with a local anesthetic drug under the rhomboid intercostal muscle and the serrates anterior muscle before surgery.

Interventions

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Rhomboid intercostal block

Patients will be injected with a local anesthetic drug under the rhomboid intercostal muscle before surgery.

Intervention Type PROCEDURE

Rhomboid intercostal and subserratus plane block

Patients will be injected with a local anesthetic drug under the rhomboid intercostal muscle and the serrates anterior muscle before surgery.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Patients in American Society of Anesthesiologists (ASA) classes I, II and III for whom VATS is planned

Exclusion Criteria

* Known or suspected local anesthetic allergy
* coagulopathy
* injection site infection
* history of thoracic surgery
* serious neurological or psychiatric disorder
* severe cardiovascular disease
* liver failure
* renal failure
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Uludag University

OTHER

Sponsor Role lead

Responsible Party

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Ferhat Ustuner

Research Assistant Doctor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Hastane

Bursa, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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UludagThorax

Identifier Type: -

Identifier Source: org_study_id

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