Clinical trials: Gastrointestinal Decompression
Esophageal Fistula
Esophageal Fistula After Anterior Cervical Decompression and Fusion
This study aims to evaluate the incidence, risk factors, and preventive measures of esophageal fistula following anterior cervical decompression and fusion.
- Trial name
- ACDF (NCT06536738)
- Testing
- esophageal repair
- Volunteers
- 5 people
- Sponsor
- Taizhou Hospital
Colonic Cancer, Rectal Cancer
Transanal Decompression Tube Versus Stent for Acute Malignant Left-sided Colonic and Rectal Obstruction
The purpose of this study is to compare the clinical outcomes of transanal decompression tube as a bridge to surgery with stent as a bridge to surgery for acute malignant left-sided colonic and rectal obstruction.
- Trial name
- NCT02585271
- Testing
- Transanal decompression tube, Stent
- Where
- China
- Volunteers
- 8 people
- Sponsor
- Xuzhou Central Hospital
Gastric/Gastroesophageal Junction (g/Gej) Cancer
JNT Versus TNT to Guided OGT-overlap Oesophagojejunostomy
Gastric/gastroesophageal junction (G/GEJ) cancer patients who underwent laparoscopic total gastrectomy (LTG) were eligible for this study
- Trial name
- NCT06412575
- Testing
- JNT Guided OGT-overlap Oesophagojejunostomy, TNT Guided OGT-overlap Oesophagojejunostomy
- Where
- China
- Volunteers
- 108 people
- Sponsor
- Nanfang Hospital, Southern Medical University
Healthy
The Effect of the SBS Decompression Technique on Gastrointestinal Symptoms During the Menstrual Cycle
Determining the effects of a single application of the sphenobasilar synchondrosis (SBS) decompression technique, on gastrointestinal symptoms during the menstrual cycle is an area that lacks of evidence and proper studies.
- Trial name
- NCT05922189
- Testing
- SBS Decompression Technique
- Where
- Portugal
- Volunteers
- 60 people, healthy volunteers welcome
- Sponsor
- Escola Superior de Tecnologia da Saúde do Porto
Colon Cancer, Obstruction
Outcome of Neoadjuvant Chemotherapy for Obstructive Colon Cancer
In this study, patients with obstructive colon cancer will be divided into two groups; in the control group, curative surgery will be performed within 2 weeks after successful SEMS placement, and in the experimental group, 3…
- Trial name
- NCT04889820
- Testing
- Neoadjuvant chemotherapy, Adjuvant chemotherapy, Curative resection
- Volunteers
- 204 people
- Sponsor
- The Catholic University of Korea