Actively Recruiting
A Multicenter, Randomized Controlled Trial to Evaluate the Efficacy of Thread Embedding Acupuncture in Reducing Postoperative Ileus After Colorectal Cancer Surgery
Led by Northern Jiangsu People's Hospital · Updated on 2025-07-18
300
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the effectiveness and safety of thread embedding acupuncture (TEA) to help speed up gastrointestinal recovery after laparoscopic colorectal cancer surgery. This multicenter, randomized controlled trial focuses on patients with colorectal cancer, specifically assessing the time until first flatus as the primary outcome. Secondary outcomes include time to first bowel movement, ability to tolerate oral intake, length of hospital stay, and quality of life reported by patients. Participants are divided into three groups: one receiving thread embedding acupuncture combined with electroacupuncture, another receiving electroacupuncture alone, and a control group receiving standard care without acupuncture. Thread embedding acupuncture involves placing absorbable sutures under the skin at specific acupoints shortly after surgery, followed by electroacupuncture sessions at the same points over the next three days. All acupuncture procedures are performed by licensed professionals following strict protocols. During the study, participants will be monitored for gastrointestinal recovery progress through various assessments including time to first flatus and defecation, oral intake tolerance, and patient questionnaires on quality of life. The study also tracks hospital stay length and monitors for any complications. Participation spans the postoperative period up to 96 hours after surgery, with safety and recovery outcomes carefully recorded by the research team.
CONDITIONS
Brief Title
Effect of Thread Embedding Acupuncture on Postoperative Ileus Recovery After Colorectal Cancer Surgery: A Multicenter Randomized Controlled Trial
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 18 and 80 years
- Diagnosed with stage I to III colorectal cancer
- Scheduled for elective laparoscopic colorectal resection
- ASA Physical Status I to III
- Ability to provide informed consent
You will not qualify if you...
- History of prior major abdominal surgery
- Emergency or palliative surgery
- Combined organ resection or open conversion
- Severe postoperative complications such as anastomotic leak or gastrointestinal bleeding
- Severe cardiac, hepatic, renal, or psychiatric conditions
- Refusal to undergo acupuncture
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Day of surgery
Participants undergo elective laparoscopic colorectal resection as part of their standard care.
1 visit (in-person)
Duration - Up to 4 days post surgery
Participants receive thread embedding acupuncture and electroacupuncture or electroacupuncture alone at specified acupoints starting 2 hours after surgery and continuing at 24, 48, and 72 hours postoperatively.
4 visits (in-person) within 72 hours after surgery
Duration - Up to 4 days after surgery
Participants are monitored for recovery outcomes including time to first flatus up to 96 hours after surgery.
Visits coinciding with treatment visits and assessments up to 96 hours
Trial Site Locations
Total: 1 location
1
Northern Jiangsu People's Hospital
Yangzhou, Jiangsu, China, 225000
Actively Recruiting
Research Team
D
Daorong Wang, Doctor
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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