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Search / Trial NCT06275165

The Effects of Acupressure on Improving Postoperative Gastrointestinal Symptom Distress in Esophageal Cancer Patients

Launched by CHEN, CHIA-CHEN · Feb 17, 2024

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Gastrointestinal Symptom Distress Acupressure

ClinConnect Summary

This clinical trial is studying how acupressure, a gentle form of pressure applied to specific points on the body, might help improve gastrointestinal symptoms in patients who have undergone surgery for esophageal cancer. Participants are divided into two groups: one group receives regular medical care along with acupressure for five days after their surgery, while the other group only receives regular care. The main goal is to see if the group that receives acupressure reports less discomfort from gastrointestinal issues compared to the control group.

To be eligible for this trial, participants need to be hospitalized men or women aged 65 to 74 who agree to take part, have a confirmed diagnosis of esophageal cancer, and require nutritional support after their surgery. However, the trial excludes pregnant or breastfeeding women, individuals with certain recent medical conditions, and those with unstable health issues. If you join the study, you can expect to receive either acupressure or regular care, and your symptoms will be assessed to determine if the acupressure made a difference. This research is important as it could help improve recovery experiences for future patients.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Hospitalized men and women who agree to participate in this study
  • Patients diagnosed with esophageal cancer based on pathological tissue section results
  • Nutritional support through jejunostomy in post esophagectomy patients
  • A sufficient level of education to understand study procedures and be able to communicate with site personnel
  • Exclusion Criteria:
  • Pregnant or lactating women
  • Diagnosed and treated for peripheral vascular disease within 3 months prior to surgery.
  • Those with unstable vital signs and septicemia infection after surgery.
  • Those who are suffering from blood diseases with abnormal coagulation function, or Currently taking anticoagulant drugs.

About Chen, Chia Chen

Dr. Chia-Chen Chen is a dedicated clinical trial sponsor with a strong commitment to advancing medical research and improving patient outcomes. With extensive expertise in the design and execution of clinical studies, Dr. Chen leads initiatives that focus on innovative therapies and evidence-based practices. Her collaborative approach fosters partnerships with healthcare professionals and research institutions, ensuring rigorous adherence to regulatory standards and ethical guidelines. Through her leadership, Dr. Chen aims to facilitate the development of groundbreaking treatments that address unmet clinical needs.

Locations

Taoyuan, , Taiwan

Patients applied

0 patients applied

Trial Officials

Chia-Chen Chen

Principal Investigator

Chang Gung Memorail Hospital

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported