Clinical trials: Incisions, Surgical
Supratentorial Tumors
Comparison of Systemic Opioid (Morphine) and Pre-Incision Bilateral Scalp Nerve Block for Pain Management in Craniotomy Patients
The goal of this randomized controlled clinical trial is to compare the effectiveness of systemic opioids versus pre-incision bilateral scalp nerve block in managing intraoperative noxious stimuli and postoperative pain in adult…
- Trial name
- NCT07425678
- Testing
- Scalp nerve block, Morphine, Lidocaine
- Where
- Pakistan
- Volunteers
- 62 people
- Sponsor
- Aga Khan University
Hemorrhoid Surgery, Liposome Bupivacaine
The Efficacy and Safety of Liposomal Bupivacaine in Relieving Postoperative Pain After Hemorrhoid Surgery
Hemorrhoids represents the most prevalent condition among anorectal disorders. Due to the unique anatomical characteristics of the perianal region, patients frequently experience severe postoperative pain, which may lead some…
- Conditions
- Hemorrhoid Surgery, Liposome Bupivacaine, Pain Management, Local Infiltration
- Trial name
- NCT07442539
- Testing
- Bupivacaine hydrochloride, Liposomal bupivacaine plus bupivacaine
- Where
- China
- Volunteers
- 156 people
- Sponsor
- Beijing Tiantan Hospital
Keloid, Scar
Safety and Efficacy of AIV001 on Scar Formation and Keloid Recurrence Following Keloidectomy
To evaluate the saftye and effectiveness of AIV001 treatment on scar formation and/or keloid scar recurrence following keloidectomy.
- Conditions
- Keloid, Scar, Incision, Excision Margin
- Trial name
- NCT04827875
- Testing
- AIV001
- Where
- 4 sites in United States
- Volunteers
- 25 people
- Sponsor
- AiViva BioPharma, Inc.
HERNIA, VENTRAL
ProLOVE - Prospective Randomized Study of Midline Incisional Hernia Treatment
This purpose of this study is to compare the recovery after an operation of an incisional hernia within the limits of the rectus muscles of the abdominal wall.
- Trial name
- ProLOVE (NCT00472537)
- Testing
- Retromuscular Mesh repair of midline incisional hernia, Laparoscopic repair of midline incisional hernia
- Where
- 7 sites in Sweden
- Volunteers
- 157 people
- Sponsor
- Skane University Hospital
Incisional Hernia
Mini- or Less-Open Sublay Operation (MILOS) of Incisional Hernias
Prospective non-randomized observational register study of all elective symptomatic incisional hernias operated on in the Hernia Center of Reference of Gross Sand Hospital using the novel endoscopic assisted Mini- or Less-Open…
- Trial name
- NCT03133000
- Volunteers
- 615 people
- Sponsor
- Gross Sand Hospital
High Grade Glioma
Glioma Supra Marginal Incision Trial
G-SUMIT is a pilot, phase II,randomized controlled trial to evaluate the feasibility of performing a large-scale trial in patients undergoing surgery for first-time diagnosis of high grade glioma (HGG) in a surgically favorable…
- Trial name
- G-SUMIT (NCT04737577)
- Testing
- Supramarginal resection, Conventional (i.e. GTR) resection
- Where
- 6 sites in United States, Canada
- Volunteers
- 44 people
- Sponsor
- Sunnybrook Health Sciences Centre
Dry Eye
Effects of Cataract Extraction Surgery and Limbal Relaxing Incision on Corneal Sensation and Dry Eye
This is a multicenter evaluation of the effects of the cataract extraction and limbal relaxing incisions (LRI) on corneal sensation and dry eye signs and symptoms.
- Trial name
- NCT01161771
- Testing
- Cataract Surgery and Limbal relaxing incision
- Where
- United States
- Volunteers
- 32 people
- Sponsor
- Allergan
Myopia, Myopic Astigmatism
Machine Learning Prediction of 1-Year Refractive Error After SMILE
This retrospective single-center observational study is designed to develop and internally validate a multi-output machine learning model for predicting 1-year postoperative refractive prediction error after small incision…
- Conditions
- Myopia, Myopic Astigmatism, Refractive Error - Myopia Axial
- Trial name
- SMILE (NCT07478419)
- Where
- China
- Volunteers
- 1,100 people
- Sponsor
- Tongji University
Colorectal Cancer, Colon Cancer
Oncologic Outcomes of Single-incision Versus Conventional Laparoscopic Surgery for Colorectal Cancer
This study is designed to investigate long-term oncologic outcomes of single-incision laparoscopic surgery (SILS) compared to conventional laparoscopic surgery (CLS) for colorectal cancer.
- Conditions
- Colorectal Cancer, Colon Cancer, Rectal Cancer
- Trial name
- CSILS (NCT04527861)
- Testing
- Single-incision Laparoscopic Surgery, Conventional Laparoscopic Surgery
- Where
- 11 sites in China
- Volunteers
- 710 people
- Sponsor
- Ruijin Hospital
Surgical Site Infection
Roles of Prophylactic Subcutaneous Drain in Preventing Surgical Site Infection in Surgical Wound After Abdominal Surgery
Surgical site infections (SSI) pose a common challenge in the field of surgery. Current evidence and literature do not provide clear consensus whether the use of subcutaneous drainage will help reduce the incidence of SSI in…
- Trial name
- NCT06063629
- Testing
- Subcutaneous drain, No drain
- Volunteers
- 180 people
- Sponsor
- Queen Savang Vadhana Memorial Hospital, Thailand
Surgical Site Infection, Groin Hernia
Prophylactic Antibiotics in Groin Hernioplasty
The role of prophylactic antibiotics in preventing surgical site infections (SSI) for clean procedures like groin hernia repair remains controversial.
- Conditions
- Surgical Site Infection, Groin Hernia, Hernioplasty
- Trial name
- NCT07111702
- Testing
- Cefazolin
- Where
- Yemen
- Volunteers
- 100 people
- Sponsor
- Sana'a University
Incisional Hernia
Audit of the EVEREG Incisional Hernia Registry (AUDHIT)
Objective: The objective of the study is to verify and validate the data collected in the EVEREG Incisional Hernia Surgery Registry between 2012 and 2018 through an audit process.
- Trial name
- AUDHIT (NCT03899012)
- Testing
- Incisional Hernia Surgery
- Where
- Spain
- Volunteers
- 337 people
- Sponsor
- Hospital Universitari Joan XXIII de Tarragona.
Surgical Wound, Knee Arthroplasty
Skin Closure in Prosthetic Joint Surgery: Comparative Evaluation of the "Barbed Sutures and Skin Glue" Technique (Cica-Pro)
The choice of skin closure (staples vs. monofilament sutures vs. barbed sutures/adhesive) is critical for wound healing quality in prosthetic surgery (hip and knee).
- Conditions
- Surgical Wound, Knee Arthroplasty, Hip Arthroplasty
- Trial name
- Cica-Pro (NCT07749495)
- Testing
- primary knee replacement, Primary hip replacement.
- Volunteers
- 400 people
- Sponsor
- Groupe Hospitalier Diaconesses Croix Saint-Simon
Surgical Site Infections, Nosocomial Infection
Nasal Photodisinfection in All Patients Presenting for Surgery for a Wide Range of Surgical Procedures
This is a Phase 2 single-center, open-label, single-arm, study of a microbiological endpoint using antimicrobial photodynamic therapy (aPDT) for nasal disinfection in all patients (universal) presenting for surgery at an acute…
- Conditions
- Surgical Site Infections, Nosocomial Infection, Healthcare Associated Infections
- Trial name
- BENEFIT-PDT (NCT05090657)
- Testing
- methylene blue 0.01%/chlorhexidine gluconate 0.25% + light activation
- Where
- United States
- Volunteers
- 322 people
- Sponsor
- Ondine Biomedical Inc.
Incisional Pain
Continuous Transversus Abdominis Plane Nerve Block for Postoperative Analgesia
Research study to determine if putting local anesthetic through one or two tiny tubes next to the nerves that go to the area the patients are having surgery on (abdomen or pelvis), will improve pain control following surgery.
- Trial name
- NCT00944151
- Testing
- TAP Catheter and Infusion of Study Solution
- Where
- United States
- Volunteers
- 20 people
- Sponsor
- University of California, San Diego
Refractive Surgery
Risk Factors for Progressive Suction Loss in Corneal Refractive Surgery
The goal of this Prospective observational studiesis to Characteristics of progressive suction loss.
- Trial name
- NCT06264804
- Where
- China
- Volunteers
- 800 people, healthy volunteers welcome
- Sponsor
- Yifeng Yu
Hernia, Obesity
Evaluation of Surgisis Gold Graft for Incision Reinforcement After Open Bariatric Surgery
The primary objective is to compare the effectiveness of the Surgisis Gold Graft to suture closure alone in preventing an incisional hernia after open bariatric surgery.
- Trial name
- NCT00274625
- Testing
- Surgisis Gold Graft, Control
- Where
- 2 sites in United States
- Volunteers
- 402 people
- Sponsor
- Cook Group Incorporated
Hernia, Hernia, Ventral
Preoptimisation in Ventral Hernia Surgery
The study is a multicentre, single-blinded, randomised controlled trial. Ventral hernia patients with an aperture width between four and eight centimetres are randomised to either participation in a multimodal preoptimisation…
- Conditions
- Hernia, Hernia, Ventral, Hernia Incisional, Hernia, Umbilical
- Trial name
- PreOpt (NCT07316426)
- Testing
- preoptimisation programme
- Where
- 5 sites in Sweden
- Volunteers
- 130 people
- Sponsor
- Umeå University
Surgical Site Infection
Wound Protector Dual-ring Alexis® in Pancreaticoduodenectomy
Surgical site infection (SSI) is a leading cause of preventable morbidity and mortality in North America and worldwide. This condition has consistently been reported to account for up to 25% of all healthcare-associated…
- Trial name
- PALEXIS (NCT03820648)
- Testing
- Alexis, Standard 3M™ Steri-Drape 2
- Where
- Italy
- Volunteers
- 212 people
- Sponsor
- Azienda Ospedaliera Universitaria Integrata Verona
Surgical Wound
A Comparative Efficacy and Safety Study Between Two Silver Containing Dressings In Post-Op Wound Healing
Study objective: The objective of this study is to evaluate through clinical criteria the clinical efficacy and safety of BCT Silver Bandage role in obstetrical and gynecological wound healing is as effective and safe as Aquacel®…
- Trial name
- NCT01605968
- Testing
- BCT Silver Bandage, Aquacel® Ag. Dressing
- Where
- Taiwan
- Volunteers
- 38 people
- Sponsor
- Bio-medical Carbon Technology Co., Ltd.
The first 1,020 results can be paged through. Add a filter or change the sort order to reach the rest.