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Healing Surgical Wounds clinical trials

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NCT ID: NCT06328413 Completed - Pain Clinical Trials

L-PRF vs PBM on Extraction Socket Healing

Start date: April 20, 2020
Phase: N/A
Study type: Interventional

The aim of this study is to compare leukocyte and platelet-rich fibrin (L-PRF) and photobiomodulation (PBM) applications, which have been repeatedly reported to be superior to control groups, in terms of pain, soft tissue and bone healing in tooth extraction sockets.

NCT ID: NCT05863728 Completed - Periapical Diseases Clinical Trials

Post-Operative Evaluation of Endodontic Microsurgeries Done Using a Piezoelectric Ultrasonic Technique: An in Vivo Study

Start date: January 1, 2020
Phase: N/A
Study type: Interventional

The aim of the study was to evaluate the effect of Piezosurgery and Trephine bur as cutting tools on post-operative sequelae including pain and swelling following guided endodontic microsurgeries.

NCT ID: NCT05375357 Completed - Clinical trials for Healing Surgical Wounds

Platelet Rich Fibrin in Soft Tissue Healing After Implant Uncovering

Start date: April 20, 2021
Phase: N/A
Study type: Interventional

This study represents a prospective, controlled and randomized clinical trial assessing the effects of L-PRF on the healing time of the donor area and on the patient's postoperative morbidity in the 4 weeks following the Apically Positioned Flap (APF) procedure in the uncovering phase of two-stage implants. A total of 40 patients were recruited and divided into two groups. The implant uncovering procedure in the test group was performed with APF and application of L-PRF on the donor area. Patients in the control group, on the other hand, were treated with APF alone, leaving the donor area to heal by secondary intention.

NCT ID: NCT05356546 Completed - Cardiac Disease Clinical Trials

TYRX™ Pocket Health Study

Start date: May 31, 2022
Phase:
Study type: Observational

Medtronic, Inc. is sponsoring the TYRX™ Pocket Health Study to evaluate the histological and morphometric parameters of the device capsule in participants who underwent a cardiovascular implantable electronic device (CIED) procedure with a TYRX™ Absorbable Antibacterial Envelope and are returning for a CIED replacement procedure.

NCT ID: NCT04531800 Completed - Infection Clinical Trials

Surgical Management of Medication Related Osteonecrosis of the Jaws With Concentrated Growth Factor

Start date: May 1, 2016
Phase: N/A
Study type: Interventional

The purpose of this present study was to evaluate the efficiency of the growth factors delivered by concentrated growth factor (CGF) on the healing process of osteoporotic patients with medication-related osteonecrosis of the jaws (MRONJ). This randomized controlled study composed of osteoporotic female patients who were treated with oral bisphosphonates (BPs) and diagnosed with MRONJ. For the CGF group, each patient was treated with local application of CGF at the surgical site after removing the necrotic bone while the surgical area was only primarily closed as traditional surgical therapy for the control group. The patients underwent clinical examinations for 6 months postoperatively to check the presence of infection and dehiscence.

NCT ID: NCT04514263 Completed - Quality of Life Clinical Trials

Oral Biopsies: Evaluation of the Post-surgical Discomfort

Start date: January 8, 2018
Phase:
Study type: Observational

Aim of this study is to evaluate the post-operative course in patients undergoing diagnostic or therapeutic oral mucosal biopsies. To evaluate the wound healing, all variables connected with the surgery (including post-operative complications) were recorded. To evaluate the psychological and behavioral impact of the post-operative discomfort, two survey tools were administered: OHIP-14 and visual number scale of pain (VNS) were administered at 6h, 7 days and 21 days after biopsy.

NCT ID: NCT03988972 Completed - Clinical trials for Healing Surgical Wounds

Efficacy of Diathermy on Healing Power of Cesarean Section Scar

EDHPCS
Start date: February 6, 2019
Phase: N/A
Study type: Interventional

To compare the effects of electro-surgery on healing power as a primary outcome (from skin to the peritoneum. And volume of blood loss, incision time and postoperative surgical wound pain as secondary outcomes.

NCT ID: NCT03563625 Completed - Clinical trials for Healing Surgical Wounds

Local Wound Infiltration Versus Caudal Block on Wound Infection and Healing in Paediatrics Inguinal Herniotomy

Start date: November 4, 2017
Phase: N/A
Study type: Interventional

The aim of the present study is to assess effect of local wound infiltration in comparison with caudal block by bupivacaine 0.25% after inguinal herniotomy in pediatrics on: Wound infection and healing (primary outcome) and postoperative analgesia (secondary outcome).

NCT ID: NCT03556163 Completed - Periodontitis Clinical Trials

Modified Vertical Internal Mattress Suture Versus Simple Loop Interrupted Suture.

Start date: December 1, 2016
Phase: N/A
Study type: Interventional

Aim of study was clinical comparative evaluation of using modified vertical internal mattress suturing technique and simple loop interrupted suturing technique in the outcome of modified Widman flap surgery for the management of chronic periodontitis.