30
Participants
Start Date
November 15, 2021
Primary Completion Date
June 1, 2022
Study Completion Date
August 30, 2022
application of PRF
PRF will be randomly administered into one group of patients undergoing any extractions group A (Right after the extraction) Group B will be a control group in which extraction sockets will be left to heal with the natural blood clot. Consenting patients will be assigned into groups randomly and not informed which group they were placed into. The PRF will be administered obtained from a tube of 10 ml blood and no material will be placed in the control group. The progress of healing and post-operative complications will be tracked over a period of 7 days with patients being called for follow-up on days 3, 5 and 7
application of conventional surgicel
it will be a control group in which extraction sockets will be left to heal with the natural blood clot.
Department of Oral and Maxillofacial Surgery, Dow University of Health Sciences, Karachi
Dow University of Health Sciences
OTHER