Clinical trials: Colostomy
Anesthesia, ERAS
Impact of General Anesthesia v/s Spinal Anesthesia on ERAS Parameters in Intestinal Stoma Reversal
Randomized, Interventional ,Open labeled, Parallel Assignment and Superiority trial.
- Conditions
- Anesthesia, ERAS, Surgical Stomas, Ileostomy - Stoma
- Trial name
- SPIGERAS (NCT06226753)
- Testing
- Type of anaesthesia used
- Where
- India
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- All India Institute of Medical Sciences, Bhubaneswar
Ileostomy, Colostomy
SCOPE - Single-Point Classification Observational Peristomal Evaluation
Study to create an ostomy dataset and collect stoma photos to enable evaluation of images digitally versus an in-person ostomy skin assessment.
- Conditions
- Ileostomy, Colostomy, Urostomy
- Trial name
- NCT06614491
- Where
- 4 sites in Brazil, Colombia
- Volunteers
- 605 people
- Sponsor
- ConvaTec Inc.
Ileostomy, Colostomy
Diverting Ileostomy and Transverse Colostomy Comparative Study
Protective diverting stomas are frequently constructed after low anterior resection or colorectal anastomosis to mitigate the consequences of anastomotic leakage, one of the most feared complications in colorectal surgery.
- Conditions
- Ileostomy, Colostomy, Colorectal Surgery
- Trial name
- NCT07283952
- Testing
- Diverting ileostomy, Diverting Transverse Colostomy
- Volunteers
- 36 people
- Sponsor
- Assiut University
Colostomy, Ileostomy
User Evaluation of the Peristomal Skin Condition in Ostomates Using ConvaTec Moldable Technology™
The primary aim of this study is to demonstrate the maintenance of healthy peri-stomal skin over a two month period in subjects who use ConvaTec Moldable Technology™ Skin Barriers as part of their standard protocol of care…
- Conditions
- Colostomy, Ileostomy, Urostomy
- Trial name
- OSMOSE (NCT02499588)
- Testing
- Esteem Plus with ConvaTec Moldable Technology, Natura with ConvaTec Moldable Technology, Natura Accordion with ConvaTec Moldable Technology
- Where
- Poland
- Volunteers
- 600 people
- Sponsor
- ConvaTec Inc.
Left-sided Colorectal Cancer Complicating Acute Obstruction
Evaluation of The Efficacy And Safety of PD-1 + IL-2 Combined With Capox Treatment After Loop Colostomy Surgery in Left-sided Colorectal Cancer Patients Complicating Acute Obstruction
Evaluation of The Efficacy And Safety of Tislelizumab (PD-1) Monoclonal Antibody + IL-2 Combined with Capox Treatment Following Loop Colostomy Surgery in Left-sided Colorectal Cancer Patients Complicating Acute Obstruction
- Trial name
- NCT06394791
- Testing
- Tislelizumab + IL-2 Combined with Capox
- Volunteers
- 27 people
- Sponsor
- The First Affiliated Hospital with Nanjing Medical University
Ileostomy - Stoma, Colostomy Stoma
Assessment of New Enhanced Ostomy Device in Real-life Settings in Subjects Having a Stoma
The study investigates the performance of a new adhesive with regard to the skin condition
- Trial name
- NCT03770078
- Testing
- Test Product A
- Where
- 4 sites in Denmark, Sweden
- Volunteers
- 23 people
- Sponsor
- Coloplast A/S
Colon Cancer
Neoadjuvant Chemotherapy for Obstructive Colon cancER First Treated by cOlostomy
The aim of this study is to determine whether chemotherapy prior to tumor removal (neoadjuvant chemotherapy), in patients undergoing treatment for colon cancer in occlusion (CCO), would improve the rate of patients able to…
- Trial name
- COnCERTO (NCT06107920)
- Testing
- Neoadjuvant chemotherapy
- Where
- 28 sites in France
- Volunteers
- 232 people
- Sponsor
- University Hospital, Rouen
Rectal Neoplasms, Quality of Life
Surviving Rectal Cancer at the Cost of a Colostomy International Validation of the Colostomy Impact Score
The formation of a colostomy following surgery for rectal cancer changes body image, challenges patient practical skills and threatens quality of life.
- Conditions
- Rectal Neoplasms, Quality of Life, Colostomy Stoma
- Trial name
- NCT03516916
- Testing
- Questionnaires on HRQoL and sociodemography
- Where
- Denmark
- Volunteers
- 3,750 people
- Sponsor
- Aarhus University Hospital
Colostomy - Stoma, Ileostomy - Stoma
The Effect of Preoperative Stoma Simulation on Anxiety and Postoperative Adaptation
The majority of patients (60-70%) develop high levels of anxiety before surgery. Surgical patients may experience feelings of anxiety due to insufficient information and counseling before surgery and potential changes in the body…
- Trial name
- NCT06737887
- Testing
- Stoma simulation
- Where
- Turkey (Türkiye)
- Volunteers
- 58 people
- Sponsor
- Kocaeli University
Colostomy Stoma
NM-IL-12 (rHuIL-12) in Subjects With Open Surgical Wounds
The purpose of this study is to determine the safety and tolerability of NM-IL-12 relative to standard of care (SOC; control) in subjects with open surgical wounds.
- Trial name
- NCT02544061
- Testing
- NM-IL-12
- Where
- 3 sites in United States
- Volunteers
- 18 people, healthy volunteers welcome
- Sponsor
- Neumedicines Inc.
Ostomy - Ileostomy or Colostomy
Ostomy Readmission Reduction Program
The purpose of this study is to reduce complications like peristomal skin issues, stoma-related problems, dehydration, and other preventable factors that can lead to re-hospitalization within the first 30 days after surgery.
- Trial name
- NCT06956274
- Testing
- Preoperative Telehealth, Measure Ostomy Output
- Where
- United States
- Sponsor
- Cedars-Sinai Medical Center
Ileostomy - Stoma, Colostomy
A Clinical Investigation Evaluating and Understanding Parameters Affecting the Performance of Ostomy Products
The aim of the study is to obtain an understanding of relevant parameters affecting the performance of ostomy products.
- Trial name
- NCT02517541
- Testing
- SenSura Mio Convex Soft
- Where
- 9 sites in United States, Netherlands and 2 more
- Volunteers
- 74 people
- Sponsor
- Coloplast A/S
Parastomal Hernia
Evaluation of the Parietex TM Parastomal No Hole Mesh for Repair of Parastomal Hernias in End-colostomies
Short Title: PHARAOH study: LAPAROSCOPIC PARASTOMAL HERNIA REPAIR WITH A NO HOLE MESH. Objectives: Evaluation of operative complications, colostomy function, Quality of Life and recurrence rate after laparoscopic repair of…
- Trial name
- PHARAO (NCT04966065)
- Testing
- Parietex Parastomal mesh
- Where
- Belgium
- Volunteers
- 10 people
- Sponsor
- University Hospital, Ghent
Stoma Site Incisional Hernia
A Prospective Clinical Trial of Colostomy-replacement Combined With Bio-mesh Placement in the Prevention of SSIH
The goal of this clinical trial is to explore the safety and effectiveness of stoma reversal combining bio-mesh placement in patients with high risk of stoma site incisional hernia (SSIH).
- Trial name
- NCT05627284
- Testing
- Stoma reversal with bio-mesh placement
- Where
- China
- Volunteers
- 58 people
- Sponsor
- The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School
Ostomy - Ileostomy or Colostomy, Canser
The Effect of Ostomy Care Education Applied With the Teach-Back Method to Ostomy-Opened Individuals on Self-Care Power, Ostomy Adjustment, and Anxiety
The aim of this study is to examine the effect of ostomy care education-delivered to patients who have undergone ostomy surgery using the Teach-back method on patients' self-care ability, ostomy compliance, and anxiety levels.
- Conditions
- Ostomy - Ileostomy or Colostomy, Canser, Ileus, Intestinal Cancer
- Trial name
- NCT07788079
- Testing
- TEACH BACK METHOD
- Where
- Turkey (Türkiye)
- Volunteers
- 44 people
- Sponsor
- Saglik Bilimleri Universitesi
Diverticular Disease of Colon, Colostomy Complication
Comparing Hartmann's Procedure and Primary Resection With Anastomosis in Hinchey III-IV Diverticulitis: Focus on Ostomy Closure and Long-Term Outcomes
Brief Summary This multicenter study compares the effectiveness of primary anastomosis with diverting loop ileostomy to Hartmann's procedure for managing perforated sigmoid diverticulitis in stable patients.
- Conditions
- Diverticular Disease of Colon, Colostomy Complication, Colostomy - Stoma
- Trial name
- ARES (NCT06794905)
- Volunteers
- 578 people
- Sponsor
- Azienda Sanitaria Locale Napoli 2 Nord
Rectal Cancer, Rectal Tumor
Efficacy and Safety of the CG-100 Intraluminal Bypass Device
A randomized trial to assess the safety and efficacy of CG-100 for reducing stoma creation rate in subjects undergoing mesorectal excision.
- Conditions
- Rectal Cancer, Rectal Tumor, Rectal/Anal
- Trial name
- NCT04184973
- Testing
- CG-100 intraluminal bypass device, Stoma
- Where
- 10 sites in United States, Germany and 3 more
- Volunteers
- 250 people
- Sponsor
- Colospan Ltd.