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Comparison of A-PRF vs Bone Wax in Hemostasis, Pain Relief and Healing Following Exodontia

NCT05744726 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 129

Last updated 2023-02-27

No results posted yet for this study

Summary

The goal of this clinical trial is to compare the pain relief and healing effect of A-PRF and Bone-wax in patients having mandibular tooth-extractions. The main question\[s\] it aims to answer are:

In the perspective of improvement in pain and healing;

* Does A-PRF performs better than control group?
* Does Bone-wax performs better than control group?
* Healing index and Pain scale score Comparison of A-PRF and Bone-wax; if one is better than the other? Participants will be asked to give resoponse to a post-operative symptom severiety (PoSSe) scale. An investigator will score the patient's extraction for hemostasis and on healing index \[describe the main tasks participants will be asked to do, treatments they'll be given and use bullets if it is more than 2 items\]. If there is a comparison group: Researchers will compare \[insert groups\] to see if \[insert effects\].

Conditions

  • Post-Extraction Socket Hemostasis
  • Post-Extraction Socket Pain Relief
  • Post-Extraction Socket Healing

Interventions

BIOLOGICAL

A-PRF

0.5 to 1g of Advance Platelet-Rich Fibrin (A-PRF) clot for each dental socket.

COMBINATION_PRODUCT

Bone-wax

0.5 to 1g of Bone-wax for each dental socket

Sponsors & Collaborators

  • Jinnah Postgraduate Medical Centre

    collaborator OTHER_GOV

  • Altamash Institute of Dental Medicine

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-01-01
Primary Completion
2023-06-30
Completion
2023-09-30

Countries

  • Pakistan

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05744726 on ClinicalTrials.gov