Clinical trials: Post-surgical Wound Healing
Shoulder Pain
Does Meloxicam Provide as Much Pain Relief as Opioids After Shoulder Surgery?
The opioid epidemic continues to be a major concern, with orthopedic surgeons being among the top prescribers of opioids. Studies evaluating these practices found that opioids are overprescribed, even for common procedures.
- Trial name
- NCT04725357
- Testing
- Meloxicam 15 mg, Preoperative Interscalene Nerve Block, arthroscopic labral repair
- Where
- United States
- Volunteers
- 96 people, healthy volunteers welcome
- Sponsor
- Rothman Institute Orthopaedics
Postoperative Complications, Surgical Wound Infection
Acupuncture and Post-Surgical Wound Healing
The purpose of this study is to determine if acupuncture improves wound healing. Since we, the investigators at the University of California, San Francisco (UCSF), know that how much oxygen is delivered to tissue is the best…
- Conditions
- Postoperative Complications, Surgical Wound Infection, Surgical Wound Dehiscence
- Trial name
- NCT00260494
- Testing
- acupuncture
- Where
- United States
- Volunteers
- 65 people
- Sponsor
- University of California, San Francisco
Post-Surgical Complication, Breast Cancer Surgery
The Efficacy of Using Pentoxifylline in Patients Undergoing Breast Cancer Surgery
The goal of this clinical trial is to assess the efficacy of pentoxifylline in reducing postsurgical complications for breast cancer patients undergoing breast cancer surgery.
- Trial name
- NCT06087237
- Testing
- Pentoxifylline, paracetamol +ketorolac
- Where
- Egypt
- Volunteers
- 92 people
- Sponsor
- Mansoura University
Rehabilitation, Rotator Cuff
Prehabilitation Before Surgery: A Strategy To Accelerate Recovery After Rotator Cuff Repair?
A rotator cuff tear is a structural injury to one or more tendons of the rotator cuff, ranging from degenerative changes to partial or complete tears.
- Conditions
- Rehabilitation, Rotator Cuff, Prehabilitation
- Trial name
- PREHAB (NCT07820592)
- Testing
- Prehabilitation
- Where
- Chile
- Volunteers
- 30 people
- Sponsor
- Laura Castillo Vejar
Post-operative Healing Following Blepharoplasty and Ptosis Repair
Efficacy of Loteprednol Ointment Following Eyelid Surgery
Inflammation occurs after any type of incisional surgery. This study will evaluate the efficacy of Loteprednol etabonate ointment vs. Soothe ointment (vehicle) for postoperative inflammation after routine eyelid surgery.
- Trial name
- NCT01749241
- Testing
- Loteprednol etabonate ophthalmic ointment, Vehicle Ophthalmic Ointment
- Where
- United States
- Volunteers
- healthy volunteers welcome
- Sponsor
- University of California, San Diego
Surgical Site Infection, Skin Cancer
Cyanoacrylate Skin Adhesive After Mohs Surgery or Wide Local Excision
This study will compare surgical site infection after linear repair with or without cyanoacrylate skin adhesive following Mohs micrographic surgery or wide local excision.
- Conditions
- Surgical Site Infection, Skin Cancer, Wound Healing
- Trial name
- NCT07844681
- Testing
- Cyanoacrylate Skin Adhesive, Fast Gut Running Epidermal Suture Closure, Vicryl Rapide Running Epidermal Suture Closure
- Where
- 3 sites in United States
- Volunteers
- 300 people
- Sponsor
- University of Minnesota
Macular Hole
Visual Acuity and Optical Coherence Tomography One Year After ILM-flap Transposition
ILM-flap (internal limiting Membrane-flap) transposition is a new surgical option in repair of macular holes, therefore one year outcomes are needed to better evaluate that method.
- Trial name
- NCT03465865
- Testing
- optical coherence tomography
- Where
- Austria
- Volunteers
- 41 people
- Sponsor
- Vienna Institute for Research in Ocular Surgery
Blepharoptosis
Risk of Dry Eye Post Different Surgeries for Blepharoptosis Repair
Blepharoptosis, inferodisplacement of the upper eyelid, can be congenital or acquired. Acquired Blepharoptosis is usually aponeurotic, due to stretching or disinsertion of the levator aponeurosis.
- Trial name
- NCT02501187
- Testing
- Levator advancement, Müller's muscle-conjunctival resection procedure, White line advancement
- Where
- Israel
- Volunteers
- 75 people, healthy volunteers welcome
- Sponsor
- Rabin Medical Center
Wound Healing, Prevena
Prevena™ Incision Management System vs Conventional Management for Wound Healing
Comparison in abdominal wound healing after contaminated or dirty surgery with incisional negative pressure wound therapy versus standard dressing.
- Conditions
- Wound Healing, Prevena, Dirty Abdominal Surgery, Contaminated Abdominal Surgery
- Trial name
- NCT02892435
- Testing
- incisional negative pressure wound therapy, conventional dressing
- Where
- Italy
- Volunteers
- 120 people
- Sponsor
- Ospedale Misericordia e Dolce
Corneal Epithelium Defect
GenTeal in Perioperative Treatment of Laser Assisted in Situ Keratomileusis LASIK Patients
GenTeal gel is an artificial tear gel used to lubricate the surface of the eye. This study will evaluate the effect of GenTeal gel on comfort following LASIK surgery.
- Trial name
- NCT00598689
- Testing
- 0.3% hypromellose
- Where
- United States
- Volunteers
- 80 people, healthy volunteers welcome
- Sponsor
- Augusta University
Classic Bladder Exstrophy, Renal Function
Kidney Function in Patients With Bladder Exstrophy
Patients with classical bladder exstrophy undergo many surgical interventions with secondary urinary tract infections complicating their course.
- Conditions
- Classic Bladder Exstrophy, Renal Function, GFR, Proteinuria
- Trial name
- NCT02192801
- Where
- Israel
- Volunteers
- 30 people
- Sponsor
- Tel-Aviv Sourasky Medical Center
Parastomal Hernia
Risk Factors for Morbidity After Parastomal Hernia Repair
The Danish Ventral Hernia Database (DVHD) registers 37 different perioperative parameters. The aim of present study is to use large-scale data from DVHD to uncover risk factors for readmission, reoperation (any indication), death…
- Trial name
- PAHEREP (NCT01484743)
- Testing
- differences in surgical techniques
- Where
- Denmark
- Volunteers
- 199 people, healthy volunteers welcome
- Sponsor
- Zealand University Hospital
Flexor Tendon Injury
Virtual Reality Combined With Active Mobilization Post Flexor Tendon Repair
The purpose of this study is to evaluate the efficacy of combining IVR-based rehabilitation with a controlled early active mobilization protocol on functional outcomes, digit range of motion, grip strength, pinch strength and…
- Trial name
- NCT07875452
- Testing
- active mobilization, active mobilization plus IVR-based rehabilitation.
- Where
- 2 sites in Egypt
- Volunteers
- 54 people
- Sponsor
- Cairo University
Cartilage Injury of Knee
A Multicenter Trial of Sprifermin (AS902330 [Recombinant Human Fibroblast Growth Factor-18]) or Placebo After Microfracture Surgery for Cartilage Injury of the Knee
This is a Phase 2, double-blind, multicenter, randomized, placebo-controlled trial to evaluate the efficacy and safety of Sprifermin (AS902330) (recombinant human fibroblast growth factor-18 [rhFGF-18]) as an adjunct treatment to…
- Trial name
- NCT01689337
- Testing
- Sprifermin (AS902330)
- Volunteers
- 1 people
- Sponsor
- EMD Serono
Quality of Life, Wound Complications
The Benefits of the Use of a Support Bra in Women Undergoing Coronary Artery By-Pass Graft Surgery
That study have the primary purpose identify if exist difference to the healing and quality of life between women that use of a surgical support bra, common support bra and without support bra after coronary artery bypass graft…
- Conditions
- Quality of Life, Wound Complications, Pain
- Trial name
- NCT02864186
- Testing
- control, surgical support bra, common support bra
- Where
- Brazil
- Volunteers
- 190 people, healthy volunteers welcome
- Sponsor
- University of Sao Paulo
Rotator Cuff Tear Surgical Repair
H-Wave® Device Stimulation for Post-operative Rotator Cuff Repair Surgery
The goal of this intent-to-treat study is to evaluate the efficacy of H-Wave Device Stimulation following rotator cuff repair surgery.
- Trial name
- NCT07501949
- Testing
- Routine post-surgical care plus H-Wave® Device Stimulation (HWDS), Routine post-surgical care
- Where
- 4 sites in United States
- Volunteers
- 80 people
- Sponsor
- Electronic Waveform Lab
Arthroscopic Bankart Repair, Arthroscopic Shoulder Surgery
Relation Between Hand Grip and Shoulder Muscle Strength After Surgical Stabilization of Shoulder Dislocations
To investigate the correlation between shoulder lateral rotators strength (LRS) and hand grip strength (HGS) at different shoulder positions in patients following arthroscopic Bankart repair surgery for anterior shoulder…
- Conditions
- Arthroscopic Bankart Repair, Arthroscopic Shoulder Surgery, Hand Grip Strength, Rotator Cuff Strength
- Trial name
- NCT07099781
- Testing
- handheld dynamometer and hand grip dynamometer
- Where
- 2 sites in Egypt
- Volunteers
- 15 people
- Sponsor
- Cairo University
Complex Abdominal Aortic Aneurysms
Patient-Reported Quality of Life After Open Surgery for Complex Abdominal Aortic Aneurysms: A Prospective Study
STUDY DURATION: January 2026 - December 2027 Each participant will be followed for 12 months postoperatively. BACKGROUND AND RATIONALE: Complex abdominal aortic aneurysms (cAAAs)-including juxtarenal, pararenal, and suprarenal…
- Trial name
- NCT07580443
- Testing
- To assess changes in health-related quality of life (HRQoL) using the Short Form-36 (SF-36) questionnaire
- Where
- 2 sites in Switzerland
- Volunteers
- 125 people
- Sponsor
- Prouse Giorgio
Axillary Hidradenitis Suppurativa
Perforator Flaps for Axillary Hidradenitis Suppurativa
Hidradenitis Suppurativa (HS) is a recurrent inflammatory disease (< 2 episode /6 months) with 1%-4% prevalence in Europe. Suppurating lesions are painful and involve one or more regions (axilla, genitofemoral, perineum, gluteal…
- Trial name
- HS-PAX (NCT03784313)
- Testing
- skin repair by axillary perforator flaps, skin repair by secondary wound healing
- Where
- France
- Volunteers
- 88 people
- Sponsor
- Assistance Publique - Hôpitaux de Paris
Mitral Regurgitation, Tricuspid Regurgitation
Annuloplasty Rings and Band Post-Market Clinical Follow-Up Study
ARB-PMCF is a multicenter, observational study of the safety and performance of Abbott annuloplasty devices used in surgical repair of mitral and tricuspid valve regurgitation.
- Conditions
- Mitral Regurgitation, Tricuspid Regurgitation, Valvular Heart Disease
- Trial name
- ARB-PMCF (NCT04761120)
- Testing
- Abbott SJM Rigid Saddle Ring, Abbott SJM Séguin Ring, Abbott SJM Tailor Ring
- Where
- 17 sites in United States, Estonia and 5 more
- Volunteers
- 550 people
- Sponsor
- Abbott Medical Devices