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Carpal Tunnel SyndromePhase 4NCT06349824

Dextrose, Steroid, PRP: Choosing the Right Injection for CRS Relief; a RCT

A Phase 4 study testing injection Dextrose water and USG machine in people with Carpal Tunnel Syndrome, run by Sheikh Zayed Medical College at 1 site in Pakistan.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

USG guided injections to relieve carpal tunnel syndrome with dextrose water or steroid or PRP Read more about this study

Who is it for?
Ages 18 to 70 years
Conditions the study is for
Carpal Tunnel Syndrome
What is being tested?
injection Dextrose water and USG machine
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
1 sitePakistan
Study dates
10 Oct 2023to 30 Mar 2024
Phase
Phase 4
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 70 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • NA

Who cannot join

  • Na

Trial locations and contacts

1 site in 1 country.

Pakistan1 site
  • Sheikh Zayed Medical College

    Rahim Yar Khan, Punjab Province, 64200

Other trials in Pakistan

About this study

Official title: Dextrose, Steroid, PRP: Choosing the Right Injection for Long Term CRS Relief; a RCT

USG guided injections to relieve carpal tunnel syndrome with dextrose water or steroid or PRP

Being tested
injection Dextrose water, USG machine
Medical subject headings
Carpal Tunnel Syndrome

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • injection Dextrose waterDrug

    Also called PRP

    dextrose will be injected around median nerve in wrist

  • USG machineDevice

    usg guided nerve hydrdissection

Study groups in NCT06349824
Study groupRoleWhat they receive
DextroseExperimentalNot described
Receives: Device: USG machine
SteroidExperimentalNot described
Receives: Drug: injection Dextrose water; Device: USG machine
PRPExperimentalNot described
Receives: Drug: injection Dextrose water; Device: USG machine

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. VAS

    visual pain score at different intervals

    Measured: five to six months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 Apr 2024
  2. Study start10 Oct 2023
  3. Primary completion30 Mar 2024
  4. Study completion30 Mar 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
60 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06349824
Sponsor's protocol ID
004AEstb/EC/01/2022
Status last verified
Mar 2024
First submitted
31 Mar 2024
Last updated
5 Apr 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing injection Dextrose water and USG machine in people with Carpal Tunnel Syndrome, run by Sheikh Zayed Medical College at 1 site in Pakistan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 5 Apr 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

VAS (time frame: five to six months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 Apr 2024.

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