NCT07553611

Brief Summary

This study aims to evaluate the effects of ultrasound-guided interscalene, erector spinae plane, costoclavicular, and supraclavicular blocks on hemidiaphragmatic paralysis, postoperative recovery quality, opioid consumption, and pain scores.

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
88

participants targeted

Target at P50-P75 for all trials

Timeline
6mo left

Started Apr 2026

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress8%
Apr 2026Nov 2026

First Submitted

Initial submission to the registry

April 21, 2026

Completed
Same day until next milestone

Study Start

First participant enrolled

April 21, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

April 28, 2026

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 21, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

November 21, 2026

Last Updated

April 28, 2026

Status Verified

April 1, 2026

Enrollment Period

6 months

First QC Date

April 21, 2026

Last Update Submit

April 21, 2026

Conditions

Keywords

regional anaesthesiaarthroscopic shoulder surgeryhemidiaphragmatic paralysisrecovery qualityopioid consumptionpostoperative pain score

Outcome Measures

Primary Outcomes (1)

  • Hemidiaphragmatic paralysis

    Diaghragmatic excursion will be assessed using a real-time M-mode ultrasound during quite breathing, deep breathing, and sniffing maneuvers (deep breathing through the nose)

    30 minutes

Secondary Outcomes (3)

  • Recovery quality

    5 minutes

  • Postoperative analgesic consumption

    24 hours

  • Postoperative pain intensity

    24 hours

Study Arms (4)

İnterscalene group

Before the surgery, ultrasoud-guided interscalene block will be performed

Other: İnterscalene block group

Erector spinae plane block group

Before the surgery, ultrasoud-guided erector spinae plane block will be performed

Other: Erector spinae plane block group

Costoclavicular block group

Before the surgery, ultrasoud-guided costoclavicular block will be performed

Other: Costoclavicular block group

Supraclavicular block group

Before the surgery, ultrasoud-guided supraclavicular block will be performed

Other: Supraclavivular block group

Interventions

Before the surgery, ultrasoud-guided interscalene block will be performed before the surgery under standart anaesthesia monitoring

İnterscalene group

Before the surgery, ultrasoud-guided erector spinae plane block will be performed before the surgery under standart anaesthesia monitoring

Erector spinae plane block group

Before the surgery, ultrasoud-guided costoclavicular block will be performed before the surgery under standart anaesthesia monitoring

Costoclavicular block group

Before the surgery, ultrasoud-guided supraclavivular block will be performed before the surgery under standart anaesthesia monitoring

Supraclavicular block group

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

It is planned to include ASA score I-III, aged 18-65 years, who are planned to undergo elective arthroscopic surgery

You may qualify if:

  • aged 18-65 years
  • American Society of Anaesthesiology (ASA) score I-III
  • body mass index (BMI) \<30kg/m2
  • scheduled for elective arthroscopic surgery

You may not qualify if:

  • ASA score ≥4
  • BMI ≥30 kg/m2
  • declining to give written informed consent
  • controendications for block application
  • history of mental or neurological disease, severe liver and/or kidney disease
  • history of moderate or severe pulmonary disease
  • abnormal preoperative chest X-ray findings
  • scheduled for emergency surgery

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Health Sciences, Antalya Training and Research Hospital

Antalya, Muratpaşa, Turkey (Türkiye)

Location

Related Publications (2)

  • Shagufta N, Nishant S, Rajnish K, Adil A. Hemidiaphragmatic paralysis following costoclavicular versus supraclavicular brachial plexus block: A systematic review and meta-analysis. J Anaesthesiol Clin Pharmacol. 2025 Oct-Dec;41(4):587-599. doi: 10.4103/joacp.joacp_415_24. Epub 2025 Jul 9.

    PMID: 41181256BACKGROUND
  • Kim DH, Lin Y, Beathe JC, Liu J, Oxendine JA, Haskins SC, Ho MC, Wetmore DS, Allen AA, Wilson L, Garnett C, Memtsoudis SG. Superior Trunk Block: A Phrenic-sparing Alternative to the Interscalene Block: A Randomized Controlled Trial. Anesthesiology. 2019 Sep;131(3):521-533. doi: 10.1097/ALN.0000000000002841.

    PMID: 31283740BACKGROUND

Study Officials

  • Arzu Karaveli

    University of Health Sciences, Antalya Training and Research Hospital

    PRINCIPAL INVESTIGATOR
  • Bayram Akdag

    University of Health Sciences, Antalya Training and Research Hospital

    PRINCIPAL INVESTIGATOR
  • Fatih Duygun

    University of Health Sciences, Antalya Training and Research Hospital

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER GOV
Responsible Party
SPONSOR

Study Record Dates

First Submitted

April 21, 2026

First Posted

April 28, 2026

Study Start

April 21, 2026

Primary Completion (Estimated)

October 21, 2026

Study Completion (Estimated)

November 21, 2026

Last Updated

April 28, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will not share

Locations