NCT05107167

Brief Summary

Ventilator-induced diaphragmatic dysfunction is a common issue in critically ill patients. Muscle stimulation has shown to have beneficial effects in muscle groups on the extremities. A non-invasive way to stimulate the diaphragm would be the electromagnetic stimulation but it is currently unclear if that is feasible. In this proof-of-concept trial the primary aim is to show that it is possible to induce a diaphragmatic contraction leading to an inspiration with a sufficient tidal volume via an external electromagnetic stimulation of the phrenic nerve in obese patients.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
5

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Dec 2021

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

First Submitted

Initial submission to the registry

October 26, 2021

Completed
9 days until next milestone

First Posted

Study publicly available on registry

November 4, 2021

Completed
1 month until next milestone

Study Start

First participant enrolled

December 14, 2021

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 25, 2022

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 25, 2022

Completed
Last Updated

July 12, 2022

Status Verified

February 1, 2022

Enrollment Period

4 months

First QC Date

October 26, 2021

Last Update Submit

July 11, 2022

Conditions

Keywords

VIDDICUAWmuscle weakness

Outcome Measures

Primary Outcomes (1)

  • 1.Tidal volume generated by electromagentical stimulation of the phrenic nerve (ml)

    Mean tidal volume of 10 consecutively stimulations of the phrenic nerve

    approximately 15 minutes

Secondary Outcomes (11)

  • Max inspiratory flow after stimulation

    approximately 15 minutes

  • Abdominal extension maximum

    approximately 15 minutes

  • Air pressure during each breath

    approximately 15 minutes

  • Diaphragmatic thickening fraction

    approximately 15 minutes

  • Feedback/Stimulation locus relation

    approximately 15 minutes

  • +6 more secondary outcomes

Study Arms (1)

Electromagnetic stimulation

EXPERIMENTAL

Electromagnetic stimulation of the phrenic nerve.

Device: Electromagnetic stimulation

Interventions

Electromagnetic stimulation of the phrenic nerve

Electromagnetic stimulation

Eligibility Criteria

Age18 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • ≥ 18 years of age
  • American Society of Anaesthesiologists Classification I or II
  • Planned anesthesia with intubation
  • Adipositas Grade II-III

You may not qualify if:

  • Chronic lung disease
  • Preexisting diaphragmatic weakness
  • Neurologic disease with known motor weakness
  • Paralysis of the phrenic nerve
  • Contraindication for any movement in the cervical vertebrae
  • Conditions that limit the movement of the diaphragm e.g. ascites, increased intraabdominal pressure.
  • Inability to communicate in the official language
  • Infections, lesions or stricture in the neck area
  • Implanted cardiac devices e.g. pace maker, defibrillator, event recorder
  • Implanted medical pumps e.g. left ventricular assist device
  • Metal implants in the upper body
  • Preganancy

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Charité - Univiversitätsmedizin Berlin

Berlin, 10117, Germany

Location

MeSH Terms

Conditions

Muscle Weakness

Condition Hierarchy (Ancestors)

Muscular DiseasesMusculoskeletal DiseasesNeuromuscular ManifestationsNeurologic ManifestationsNervous System DiseasesPathologic ProcessesPathological Conditions, Signs and SymptomsSigns and Symptoms

Study Officials

  • Stefan J Schaller, Prof. Dr.

    Charité - Universitätsmedizin Berlin, Berlin, Germany

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
PREVENTION
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Deputy Clinical Director

Study Record Dates

First Submitted

October 26, 2021

First Posted

November 4, 2021

Study Start

December 14, 2021

Primary Completion

April 25, 2022

Study Completion

April 25, 2022

Last Updated

July 12, 2022

Record last verified: 2022-02

Data Sharing

IPD Sharing
Will share

Deidentified data can be requested on reasonable scientific request.

Shared Documents
STUDY PROTOCOL, SAP, ICF, CSR, ANALYTIC CODE
Time Frame
After publication of scientific manuscript.
Access Criteria
Deidentified data can be requested on reasonable scientific request.

Locations