Ulcerative Colitis Clinical Trials

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An Open-label Extension Study to Evaluate the Safety of the 13 mg Bimatoprost Ocular Insert

NCT02537015

This study evaluated the long-term (9-months) safety of the Bimatoprost Ocular Insert in participants with Glaucoma or Ocular Hypertension who completed study FSV5-004. All the participants received Bimatoprost Ocular Insert and wore it for approximately 3 months (12 weeks), then had that Insert removed and a new Insert placed for another 26 weeks (approximately 6 months).

Primary Open-Angle GlaucomaOcular Hypertension

ForSight Vision5, Inc.81 participantsStarted Aug 2015

Fayetteville, Arkansas, United States • Artesia, California, United States • Newport Beach, California, United States +6 more locations

UNKNOWNNA

PRF and Connective Tissue Graft in Interdental Papilla Reconstruction

NCT03899051

Interdental papilla deficiency leads to food impaction, problems with phonetics and an unaesthetic appearance. Reconstruction of the deficient papilla is therefore, important. Perusal of available literature reveals only case reports and case series in the reconstruction of interdental papilla using subepithelial connective tissue graft and platelet rich fibrin autologous graft. Therefore, the current randomized controlled clinical study is intended to compare the effect of platelet rich fibrin and subepithelial connective tissue graft on interdental papilla reconstruction.

Reconstructive Surgery

Postgraduate Institute of Dental Sciences Rohtak36 participantsStarted Dec 2018

Rohtak, Haryana, India

An Open-label Extension Study to Evaluate the Safety of the 13 mg Bimatoprost Ocular Insert

PRF and Connective Tissue Graft in Interdental Papilla Reconstruction

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