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Not yet recruitingNCT06532318Updated Aug 1, 2024

Comparative Study Between Platelet Rich Plasma and Steroid Injection in Trigger Finger Treatment

A Phase 3 interventional study of Platelet rich plasma and Pfizer Depo-medrol in Trigger Finger Disorder, sponsored by Obafemi Awolowo University Teaching Hospital. Not yet recruiting. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-08-01.

Sponsored by Obafemi Awolowo University Teaching Hospital · Phase 3, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Dec 2024, 1 year 10 months ago, but the record still lists the study as not yet recruiting.
Phase
Phase 3
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The goal of this clinical trial is to learn if platelet rich plasma works to treat early stage trigger finger in adults. It will also learn about the safety platelet rich plasma. The main questions it aims to answer are:

Does platelet rich plasma lower the pain associated with trigger finger of participants? Does it improve the hand grip strength and Q DASH score of participants? Researchers will compare platelet rich plasma to Depo-Medrol steroid (a known standard of care for early stage trigger finger) to see if platelet rich plasma works to treat early trigger finger.

Participants will:

Take platelet rich plasma or a depo-medrol steroid intralesional injection at recruitment into the intervention Visit the clinic once every 4 weeks for checkups and parameter measurements. Investigator will will keep a record of participants progress in symptom remission

02

Conditions studied

  • Trigger Finger Disorder
03

In context

Trigger Finger Disorder

93 studies on the registry are indexed under Trigger Finger Disorder; 22 are open to participants now.

This study's planned enrollment of 40 is below the median of 66 across 75 interventional studies indexed under Trigger Finger Disorder.

Browse Trigger Finger Disorder studies →

Lead sponsor

Obafemi Awolowo University Teaching Hospital is the lead sponsor of 12 studies on the registry; 5 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients who are 18year and above with mild or moderate trigger finger, who are willing to have intra-lesional administration of blood product.

No previous treatment for the affected finger.

Exclusion criteria

Exclusion Criteria:

  • Previous injection
  • Previous Surgery to that finger
  • Thrombocytopenic patients
  • Hand and finger contracture
  • Rheumatoid arthritis of the finger
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

05

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Single group
Masking
Double (Participant, Care provider)
Enrollment
40 participants (estimated)

Study arms

  • Experimental
    Group A

    Patients here will have one milliliter of freshly prepared autologus platelet rich plasma injection for the treatment of their trigger finger.

    Biological: Platelet rich plasma

  • Active comparator
    Group B

    Patients here will have one milliliter(20mg) injection of pfizer Depo-medrol(methylprednisolone acetate) injection for the treatment of their trigger finger.

    Drug: Pfizer Depo-medrol

Interventions

  • Freshly prepared autologus platelet rich plasma

  • DrugPfizer Depo-medrol

    Methylprednisolone acetate 20mg/ml injection

06

What researchers measure

Primary outcomes

  1. symptom resolution post injection

    reduction of pain using VAS and absence snapping of finger

    Time frame: 3 months

Secondary outcomes

  1. Hand grip strength

    measured grip using hand dynamomter

    Time frame: 3 month

  2. Q- DASH score

    11-item self reported disability questionnaire that consider upper extremity as one functional unit

    Time frame: 3month

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Jul 2024; primary completion for Dec 2024, 4 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Jul 29, 2024
First posted
Aug 1, 2024
StartEst.
Jul 24, 2024
Primary completionEst.
Dec 23, 2024
CompletionEst.
Jun 23, 2025
Last update
Aug 1, 2024
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 1, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06532318
Lead sponsor
Obafemi Awolowo University Teaching Hospital
Responsible party
Olorunfemi Olayiwola (orthopaedic surgeon, Obafemi Awolowo University Teaching Hospital) — Principal investigator
First posted
Aug 1, 2024
Start date
Jul 24, 2024 (estimated)
Primary completion
Dec 23, 2024 (estimated)
Completion
Jun 23, 2025 (estimated)
Last update
Aug 1, 2024

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jul 2024. You cannot join it, but the record below documents what was studied.

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Discussion

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Studies of the drug tested here: Platelet rich plasma

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