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Comparison Between IPRF With Vit. C and IPRF Alone in Management of ID'Pain

Comparison Between Injectable Platelet Rich Fibrin With Vitamin C and Injectable Platelet Rich Fibrin Alone in Management of ID'Pain

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06345092
Enrollment
40
Registered
2024-04-03
Start date
2024-04-15
Completion date
2024-08-15
Last updated
2024-11-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

TMJ Pain

Brief summary

Randomized clinical trial between 2groups,the study group to be injected in the TMJ with injectable platelet rich fibrin with vitamin C and the control group to be injected in the TMJ with injectable platelet rich fibrin alone in management of internal Temporomandibular joint derangement

Detailed description

Randomized clinical trial between 2groups,the study group to be injected in the TMJ with injectable platelet rich fibrin with vitamin C and the control group to be injected in the TMJ with injectable platelet rich fibrin alone in management of internal Temporomandibular joint derangement

Interventions

DRUGVitamin C

addition of vitamin C to IPRF

injection of IPRF alone

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

Patients with internal TMJ derangement (anterior disc displacement with reduction)

Exclusion criteria

Pathological conditions ; trauma TMJ cases or any blood diseases

Design outcomes

Primary

MeasureTime frameDescription
Pain managementat 4;8;12;16 weeksEvaluation of pain using VAS pre and post injections

Secondary

MeasureTime frameDescription
disc position using MRIat 4;8;12;16 weeksevaluation of disc position pre and post injections

Other

MeasureTime frameDescription
maximum mouth openingat 4;8;12;16 weeksmeasurement of MMO using digital caliper pre and post injections
lateral excursionat 4;8;12;16 weeksmeasurement of lateral excursion using digital caliper pre and post injections

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026