Trial · NCT05381389
Onset and Recovery of Ultrasound Guided Out-of-plane Versus In-plane Interscalene Block in Arthroscopic Shoulder Surgery
NCT05381389, Not applicable, Completed, Ain Shams University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Onset and Recovery of Ultrasound Guided Out-of-plane Versus In-plane Interscalene Block in Arthroscopic Shoulder Surgery. Trials, record NCT05381389. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT05381389
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Onset and Recovery of Ultrasound Guided Out-of-plane Versus In-plane Interscalene Block in Arthroscopic Shoulder Surgery
- NCT number
- NCT05381389
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 60 participants, actual
- Lead sponsor
- Ain Shams University
- Conditions
- Analgesia
- Interventions
- Bupivacaine Hydrochloride in-plane approach for the interscalene block, Bupivacaine Hydrochloride out of-plane approach for the interscalene block
- First posted
- 2022-05-19
- Last updated
- 2022-05-19
Source ClinicalTrials.gov
Registered outcomes8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | The onset of sensory block (time to C5 block) | 30 minutes | defined as the period between the completion of the LA administration and the loss of sensation to pin prick in C5 dermatome performed every 1 minute |
| Secondary | The procedure time | 20 minutes | time from the skin infiltration by the lidocaine till removal of the stimulating needle from the skin |
| Secondary | Progression of sensory block | over the first 20 minutes of LA injection | performed by pin prick every 5 minutes in C6, C7, C8 and T1 dermatomes |
| Secondary | The onset of motor block | 30 minutes | the period between the completion of LA administration till lack of movement of the shoulder, arm and fingers muscles assessed every 1 minute. |
| Secondary | The progression of motor block | over the first 20 minutes of LA injection | in the shoulder, arm and fingers muscles assessed every 5 minutes |
| Secondary | The duration of motor block | 24 hours | the period between the onset of motor block till complete recovery of motor function |
| Secondary | Postoperative pain score | 24 hours | Intensity of pain was monitored at rest |
| Secondary | The duration of analgesia | 24 hours | the time interval between the onset of sensory block until the first call for analgesia |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT05381389
GET https://conductscience.org/api/trials/v1/NCT05381389/registered