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Clinical Observation of Drug Retention Enema in Preventing Acute Radiation-induced Rectal Injury

Clinical Observation of Trolamine Retention Enema in Preventing Acute Radiation-induced Rectal Injury: a Real-world Multicenter Prospective Study

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06325982
Enrollment
200
Registered
2024-03-22
Start date
2024-06-11
Completion date
2025-12-31
Last updated
2024-06-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Radiation Injuries, Rectal Diseases

Brief summary

The main objective of this study was to evaluate the efficacy and safety of drug retention enema for the prevention of acute radiation rectal injury in the real world.

Detailed description

The study was a prospective, multicenter, real-world study with eligible patient data as of May 1, 2024. The prospective study was a continuous, multicenter study.

Interventions

DRUGTriethanolamine cream

Triethanolamine cream retention enema was given once every night before going to bed during radiotherapy until the end of radiotherapy. Triethanolamine cream retention enema was given once before going to bed the day after radiotherapy for 3 months. Preparation method: Pull out the syringe piston, add 15ml triethanolamine cream, add 30ml normal saline, gently pat, shake well. Specific methods of retention enema: at night before going to bed, empty urine and feces, prepare enema liquid into the syringe, connect the special catheter, and insert the other end of the special catheter into the anus (the special catheter can be applied with lubricant such as tea oil before insertion). The patient remained prone and semi-seated. Use a special catheter, insert a special catheter about 15cm from the anus, and inject enteral liquid while withdrawing, so that the liquid is retained in the rectum; The above treatment was performed before bed and retained overnight.

Sponsors

Fujian Cancer Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* There are clear indications for radiotherapy (pelvic radiotherapy or rectal radiotherapy) according to relevant guidelines; * ECOG score 0-1; * normal mind, clear consciousness; * High compliance; * Able to cooperate with the interviewer

Exclusion criteria

* Poor compliance, unwilling to participate or unable to cooperate with the interviewer; * Patients with other intestinal diseases (such as Crohn's disease, rectal ulcer, anal fissure, anal fistula, hemorrhoids, etc.) and perianal diseases; * serious heart, brain, liver, kidney disease; * Long-term immune dysfunction; * Pregnant or lactating women; * Patients who terminate treatment for various reasons.

Design outcomes

Primary

MeasureTime frameDescription
Occurrence time of acute and chronic radiation rectal injuryUp to approximately 4 monthsRTOG/EORTC criteria were used to evaluate the severity of acute and chronic radiation rectal injury. The time (days) of acute radiation rectal injury were evaluated and recorded
Evaluation of acute and chronic radiation rectal injuryUp to approximately 4 monthsRTOG/EORTC criteria were used to evaluate the severity of acute and chronic radiation rectal injury. The grading of acute radiation rectal injury were evaluated and recorded

Secondary

MeasureTime frameDescription
Clinical symptom assessmentUp to approximately 4 monthsClinical symptoms were assessed using the Simple Clinical Colitis Activity Index (SCCAI) designed by the Inflammatory Bowel Disease Research Group at the Royal Free Hospital School of Medicine. SCCAI in this study included 6 items, with a total score of 0-16. The higher the score, the more severe the symptoms.
Quality of life assessment assessed by IBDQUp to approximately 4 monthsThe quality of life index (IBDQ) was used to evaluate the quality of life of patients with inflammatory bowel disease. IBDQ included 32 questions in 4 aspects: intestinal symptoms (10), systemic symptoms (5), emotional ability (12) and social ability (5). Each question was divided into 7 grades, with a total score of 32-224 points. The higher the score, the better the quality of life. Scores above 177 indicate light, 176-121 indicate medium, and below 120 indicate heavy.

Countries

China

Contacts

Primary Contactlingdong Shao, Bachelor
1065900966@qq.com13905914564

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026