Clinical Research Directory

Flowable Resin Versus Self-Adhesive Dressing for Palatal Donor-Site Protection

This pilot randomized clinical study compared two methods for protecting the palatal donor site after harvesting a free gingival graft. Twelve adult participants were randomly assigned to receive either a hemostatic collagen sponge covered with flowable resin composite or a hemostatic collagen sponge covered with a self-adhesive oral dressing stabilized with sutures. Participants recorded pain at the palatal donor site daily for 14 days using a 0-to-10 pain scale. The study also evaluated the time required to apply each protective material and the number of days that it remained in place.

Perception of Pain During Gender Affirming Hormone Therapy

It is known from the literature that women and men differ in their perception of pain. Why this is the case has not been conclusively clarified. Sex hormones could have a significant influence on this. The study team suspects that the classic hormone status of women is responsible for the lower pain threshold compared to men. People undergoing gender affirming therapy receive biologically opposite-sex hormones in order to adapt their external appearance as well as their voice, emotional life etc. to the desired gender. The aim of this study is to longitudinally record whether the intake of opposite-sex sex hormones leads to a change in pain and perception thresholds in this patient collective. To this end, potential study participants will be informed about the study and asked whether they would like to participate before the start of hormone therapy during their first visit to the transgender outpatient clinic. If consent is given, a questionnaire on mental health (PHQ 9), a blood sample to determine the hormone status and the first QST (quantitative sensory testing) measurement are then carried out. The second measurement with blood sampling takes place 3-4 weeks after the first measurement. The 3rd and 4th measurements with blood sampling are taken 3 and 6 months respectively after the first measurement. The PHQ 9 is measured again at the time of the last measurement. Study participation ends after a total of 6 months. The blood samples, the PHQ 9 and the QST measurements have no influence on the treatment of the study participants.