Stellate Ganglion Block in Longstanding Facial Nerve Palsy Patients

December 16, 2024 updated by: Remonda zaki abdelnaeem zaki, Assiut University
The goal of the present study is to verify the efficacy of stellate ganglion block (SGB) in the treatment of facial pain

Study Overview

Status

Not yet recruiting

Intervention / Treatment

Study Type

Observational

Enrollment (Estimated)

34

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

facial nerve palsy patients

Description

Inclusion Criteria:

  • facial nerve palsy patients

Exclusion Criteria:

  1. light of a recent myocardial infarction.
  2. anticoagulant use
  3. glucoma
  4. lateral nerve palsy
  5. emphysema
  6. cardiac conduction abnormalities
  7. active infection, flu, cold
  8. uncontrolled cough
  9. Fever
  10. Very high blood pressure or if you are on blood thinners.
  11. allergic reaction to local anesthetics
  12. Primary and secondary coagulopathy.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
stellate ganglion block group
Stellate ganglion block is an injection of local anesthetic at the level of the neck to target the stellate ganglion, a sympathetic ganglion to interrupt abnormal autonomically-mediated pain in patients resistant to medical treatment
medical treatment group

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Primary outcome: Average motor conduction latency in six muscle of the face
Time Frame: 6 month
6 month

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Improved muscle tone
Time Frame: 6 months
facial muscles start to regain their strength improvement of muscle tone.
6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

December 20, 2024

Primary Completion (Estimated)

December 20, 2024

Study Completion (Estimated)

December 20, 2024

Study Registration Dates

First Submitted

December 16, 2024

First Submitted That Met QC Criteria

December 16, 2024

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

December 16, 2024

Last Verified

December 1, 2024

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

Yes

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

Yes

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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