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Active clinical trials for "Surgical Wound"

Results 211-220 of 455

A Prospective, Open, Non-controlled Clinical Investigation to Evaluate a New Negative Pressure Wound...

Acute Non Infected WoundsNon Infected Post Surgical Wounds

The investigation is designed as a prospective, open, non-controlled clinical investigation.

Completed22 enrollment criteria

Comparison of Single İncision Laparoscopic Cholecystectomy Versus Laparoscopic Cholecystectomy

Laparoscopic Surgical Procedures

The aim of this study is to compare outcomes of quality-of-life measures and evaluate the body image and cosmesis between Single Incision Laparoscopic Cholecystectomy (SILC) and Conventional Laparoscopic Cholecystectomy (CLC).Twenty eight patients underwent SILC and 30 underwent LC.Fifty-eight patients were included the study and divided into two groups. The results of the questionnaires were statistically compared.

Completed10 enrollment criteria

Comparison of Double-Flap Incision, Modified Periosteal Releasing Incision, and Coronally Advanced...

Flap Advancement

Guided Bone Regeneration (GBR) is a reliable method to augment insufficient bone volume for implant placement. Membrane exposure is a major complication which is avoided by tension free primary closure. Classically Periosteal Releasing Incision (PRI) is performed to advance the flap. The aim of this trial is to compare Double Flap Incision (DFI), Modified Periosteal Releasing Incision (MPRI) & Coronally Advanced Lingual Flap (CALF) to PRI in terms of flap advancement, postoperative pain & swelling, membrane exposure and the amount of bone gain clinically and radiographically in GBR procedures.

Completed15 enrollment criteria

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

Healing Surgical WoundsInfection

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.

Completed7 enrollment criteria

Electrocautery Versus Scalpel for Surgical Skin Incisions in Cesarean Section.

Surgical Wound Infection

To determine the risk of surgical site infection after surgical skin incision, comparing electrocautery vs. scalpel.

Completed4 enrollment criteria

Physical Activity in Patients With Gynecological Surgery

Women Who Underwent Midline IncisionGynecological Surgery

Examine whether the measurement and feedback of physical activity increase the physical activity in women who underwent midline incision, gynecological surgery

Completed5 enrollment criteria

Blood Loss During Cesarean Section. Comparing Two Techniques of Blunt Expansion of Uterine Incision:...

Blunt Expansion of the Uterine Incision

Obstetrical blood loss is an important reason of maternal morbidity and mortality. Because of the increase in the rate of cesarean section, any procedure that could help reduce blood loss during cesarean section should be investigated. The purpose of this study was to compare 2 methods of blunt expansion of the uterine incision at the time of cesarean delivery: transversal vs. cephalad-caudad.

Completed14 enrollment criteria

Co-Axial Micro-Incision Versus Co-Axial Small Incision Cataract Surgery Using the Stellaris Enhancement...

CataractAphakia

The objective of this study is to test the hypothesis that the time to reach a stable refraction is significantly shorter in eyes operated with the 1.8 mm coaxial microincision compared to eyes operated with the 2.75 mm standard incision using the Stellaris Vision Enhancement System.

Completed3 enrollment criteria

Prineo (Dermabond Protape) Versus Sutures for Full-thickness Surgical Incisions

Surgical Incisions

This is a prospective, controlled, randomized, multi-center clinical study of up to 80 subjects with full thickness surgical incisions. Each incision included in the study will be segmented into two halves; each half will be randomized to receive final skin closure with either Prineo (DERMABOND PROTAPE) or intradermal sutures. Subjects will be evaluated post-operatively at 24 hours (± 6 hours), 7 days (± 1 day), 12 - 25 days, and 90 days (± 10 days).

Completed17 enrollment criteria

Supplemental Postoperative Oxygen and Wound Infection in Morbidly Obese Patients

Surgical Wound Infection

The investigators propose to test the hypothesis that the incidence of major complications related to infection or inadequate healing is reduced in morbidly obese patients given 80% inspired oxygen during, and for 12-18 hours after, surgery compared with patients given 80% oxygen only during surgery. The primary outcome will be a composite of major complications plausibly related to infection or healing.

Terminated5 enrollment criteria
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