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Completed

NCT Number: NCT01613534

Combined Therapy in Radiation Proctopathy

The aim of this study was to compare the efficacy and safety of two treatment regimens: argon plasma coagulation (APC) alone and APC in combination with sucralfate administered for chronic hemorrhagic radiation proctopathy.

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Department of Gastroenterology and Hepatology, Medical Center for Postgraduate Education and Department of Gastroenterology, Maria Sklodowska-Curie Memorial Cancer Center and Institute of Oncology

Warsaw, Masovian Voivodeship, 02-781, Poland

About this study

Chronic radiation proctopathy (CRP) or proctosigmoiditis is a late complication of pelvic radiotherapy. Symptoms, including diarrhea, rectal bleeding, urgency, and tenesmus, are difficult to treat and adversely impact patient quality of life. Various treatments directed at the reduction of blood loss and improvement of other symptoms have been evaluated, with the most encouraging results reported for two methods: endoscopic argon plasma coagulation (APC) of radiation-induced abnormal vessels in the rectal mucosa, and administration of sucralfate, a drug believed to enhance the mucosal defense and healing when administered orally or rectally. Adequately powered randomized trials comparing various treatments are lacking, and an optimal management strategy has yet to be determined. To address this issue, we conducted a single-center, randomized, placebo-controlled, double-blind study comparing the efficacy and safety of APC alone and APC in combination with sucralfate administered orally.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • radiotherapy due to pelvic tumors completed at least three months prior to enrollment
  • presence of rectal bleeding
  • radiation-induced telangiectasia in the rectum and/or sigmoid colon on endoscopy
  • informed written consent to participate in the study

Exclusion criteria

  • history of clinically significant rectal bleeding prior to radiotherapy
  • conditions predisposing the patient to rectal bleeding including inflammatory bowel disease, tumors of the large bowel, intestinal vascular lesions (other than radiation-induced telangiectasia), and diversion of the fecal stream
  • sucralfate treatment during the two weeks prior to enrollment
  • renal insufficiency (creatinine level ≥2 mg/dl)
  • concurrent chemotherapy
  • concurrent therapy with tetracycline, fluoroquinolones, or antimycotic drugs (because of drug interaction)
  • concurrent therapy with oral anticoagulants

Treatment and study plan

Sucralfate

Drug

Argon plasma coagulation treatment followed by oral sucralfate (6 grams b.i.d.) for four weeks

Other names: Carafate, Ulgastran

Placebo

Drug

Argon plasma coagulation treatment followed by placebo administration for four weeks

Primary outcomes

  1. change in disease severity scores, as assessed using our three-item symptom scale

    Time frame: baseline vs. 16 week

    Three-item symptom scale Diarrhea - score 1: 1-3 stools/24 h; 2: 4-6 stools/24 h; 3 >6 stools/24 h Bleeding - score 0: No blood; 1: Blood on toilet paper or stool; 2: Blood in toilet bowl; 3: Heavy bleeding with clots; 4: Bleeding requiring transfusions Tenesmus/rectal pain - score 0: Absent; 1: Mild tenesmus not requiring any drug; 2: Tenesmus requiring analgesics/antispasmodics; 3: Severe tenesmus requiring everyday use of analgetics/antispasmodics.

Secondary outcomes

  1. change in endoscopic severity score

    Time frame: baseline vs. week 8 and week 16

    Endoscopic severity score of chronic radiation proctopathy:

    Normal, score 0 - Normal mucosa Mild, score 3 - Erythema and/or teleangiectasia, edema, thickening, pallor of mucosa Moderate, score 6 - Above plus friability Severe, score 9 - Ulceration and/or necrosis

  2. change in disease severity score

    Time frame: baseline vs. week 52

    disease severity score as in primary outcome measure

  3. complication rate

    Time frame: baseline to 16 weeks

Sponsors and collaborators

Lead sponsor

Maria Sklodowska-Curie National Research Institute of Oncology

Other

Collaborators

  • Medical Centre for Postgraduate Education

Registry information

Official study title

Argon Plasma Coagulation Plus Placebo or Oral Sucralfate for Chronic Radiation Proctopathy: a Randomized Placebo Controlled Trial

Important dates

Study start
2003
Primary completion
2007
Study completion
2007
First posted
Jun 7, 2012
Registry last updated
Jun 7, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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