Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06410443

Efficacy and Safety of Local Glucocorticoids for the Treatment of Acute Radiation-Induced Intestinal Injury

Led by General Hospital of Shenyang Military Region · Updated on 2025-12-24

60

Participants Needed

1

Research Sites

126 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Due to the increasing number and prolonged survival of malignant tumor patients treated with radiotherapy, the complication, such as acute radiation-induced intestinal injury, has become increasingly significant. Glucocorticoids may play a therapeutic role by regulating the inflammatory response in patients with acute radiation-induced intestinal injury. However, the conclusions of related studies were controversial.

CONDITIONS

Official Title

Efficacy and Safety of Local Glucocorticoids for the Treatment of Acute Radiation-Induced Intestinal Injury

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Grade II-III acute radiation-induced rectosigmoid injury
  • Signed informed consent
  • Age 18 years or older
  • Estimated survival time greater than 1 year
Not Eligible

You will not qualify if you...

  • Absolute contraindications to glucocorticoids
  • Glucocorticoid treatment within the past 3 months
  • Inflammatory bowel disease or infectious intestinal disease
  • Recurrence of malignant tumor
  • Colorectal cancer or metastasis
  • Severe heart or lung diseases
  • Recent history of surgery or trauma
  • Poorly controlled hyperglycemia and hypertension
  • Active tuberculosis
  • Severe gastrointestinal ulcers
  • Glaucoma
  • Psychiatric diseases
  • Pregnant or lactating

AI-Screening

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Trial Site Locations

Total: 1 location

1

Department of Gastroenterology, General Hospital of Northern Theater Command (formerly called General Hospital of Shenyang Military Area)

Shenyang, Liaoning, China, 110840

Actively Recruiting

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Research Team

X

Xingshun Qi

CONTACT

Q

Qianqian Li

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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