Comparative Study of Subcoracoid Tunnel Block Versus Costoclavicular Block

NCT ID: NCT07305584

Last Updated: 2025-12-26

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

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

70 participants

Study Classification

INTERVENTIONAL

Study Start Date

2026-01-01

Study Completion Date

2026-04-01

Brief Summary

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The purpose of this study is to compare the analgesic outcomes (time to first analgesic request, total amount of analgesic consumption, and pain scores) following the ultrasound-guided subcoracoid tunnel block or costoclavicular block for elderly patients undergoing distal upper limb surgeries.

Detailed Description

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Conditions

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Distal Upper Limb Surgeries

Keywords

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elderly Patients distal Upper Limb SurgeriesSubcoracoid Tunnel Block Costoclavicular Block

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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Group (S)

The patient will receive subcoracoid tunnel block

Group Type ACTIVE_COMPARATOR

subcoracoid tunnel block

Intervention Type OTHER

The probe will be placed with its proximal end towards the mid-clavicular point and distal end with a marker towards the apex of the axilla. A medial tilt of the probe will demonstrate the posterior and medial cords, while a slight lateral tilt of the probe will demonstrate the lateral cord. The needle entry point at the distal end of the probe will be marked. By using the in-plane technique, the needle will be advanced from a caudal to cephalad direction. The probe will be tilted medially, and the needle will be advanced to position its tip above the posterior or medial cord. The probe will be tilted laterally. The needle tip will be repositioned above the lateral cord, and the LA will be injected

Group (C)

The patient will receive costoclavicular block

Group Type ACTIVE_COMPARATOR

Costoclavicular block

Intervention Type OTHER

. The key anatomical structures will be identified under ultrasound: the pectoralis major muscle, subclavius muscle, and three brachial plexus cords (lateral, medial, and posterior) clustered tightly lateral to the axillary artery, along with the axillary artery and vein. The needle will be inserted by the in-plane technique from lateral to medial. The needle tip will be advanced through subcutaneous tissue and subclavius, aiming to land in the costoclavicular fascial plane between the cords, ideally between the lateral and posterior cords and superficial to the medial cord, without traversing neural structure by multipoint strategy, and local anesthesia will be injected.

Interventions

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subcoracoid tunnel block

The probe will be placed with its proximal end towards the mid-clavicular point and distal end with a marker towards the apex of the axilla. A medial tilt of the probe will demonstrate the posterior and medial cords, while a slight lateral tilt of the probe will demonstrate the lateral cord. The needle entry point at the distal end of the probe will be marked. By using the in-plane technique, the needle will be advanced from a caudal to cephalad direction. The probe will be tilted medially, and the needle will be advanced to position its tip above the posterior or medial cord. The probe will be tilted laterally. The needle tip will be repositioned above the lateral cord, and the LA will be injected

Intervention Type OTHER

Costoclavicular block

. The key anatomical structures will be identified under ultrasound: the pectoralis major muscle, subclavius muscle, and three brachial plexus cords (lateral, medial, and posterior) clustered tightly lateral to the axillary artery, along with the axillary artery and vein. The needle will be inserted by the in-plane technique from lateral to medial. The needle tip will be advanced through subcutaneous tissue and subclavius, aiming to land in the costoclavicular fascial plane between the cords, ideally between the lateral and posterior cords and superficial to the medial cord, without traversing neural structure by multipoint strategy, and local anesthesia will be injected.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients acceptance to share in the study.
* Patients with ASA physical status I-II.
* Patients with a body mass index (BMI): of 18.5-30 kg/m2.
* Patients undergoing distal upper limb surgeries not more than 2 hours.

Exclusion Criteria

* Patients with a history of allergic reactions or contraindications to local anesthetics.
* Patients with significant comorbidities (e.g., severe cardiovascular, neurological, or musculoskeletal disorders).
* Patients with respiratory insufficiency.
* Patients with coagulation disorders or taking drugs affecting surgical hemostasis.
* Patients with pre-existing neurological deficits
Minimum Eligible Age

65 Years

Maximum Eligible Age

85 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Zagazig University

OTHER_GOV

Sponsor Role lead

Responsible Party

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Marwa Mohamed Medhat

assistant professor of anesthesia and surgical intensive care(Principal Investigator)

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Howida A Kamal, MD

Role: STUDY_DIRECTOR

faculty of medicine,zagazig university Egypt

Locations

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faculty of medicine,zagazig university Egypt

Zagazig, , Egypt

Site Status

Countries

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Egypt

Central Contacts

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Marwa M Medhat, MD

Role: CONTACT

Phone: 01002828937

Email: [email protected]

Howida A Kamal, MD

Role: CONTACT

Phone: 01225096755

Email: [email protected]

Facility Contacts

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Marwa M Medhat, MD

Role: primary

References

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Kaya S, Sahap M, Demirtas K. Comparison of costoclavicular and lateral sagittal infraclavicular approaches in ultrasound-guided brachial plexus block. Agri. 2025 Jan;37(1):32-41. doi: 10.14744/agri.2024.34022.

Reference Type BACKGROUND
PMID: 39835953 (View on PubMed)

Other Identifiers

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ZU-IRB#1885/7-Nov-2025

Identifier Type: -

Identifier Source: org_study_id