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Completed

NCT Number: NCT00902031

Effectiveness of Docusate in Preventing/Treating Constipation in Palliative Care Patients

The purpose of this study is to determine if docusate is effective in the treatment of constipation in palliative care patients.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

CapitalCare Norwood, Edmonton, Alberta, Canada

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About this study

Palliative patients frequently experience constipation due to multiple factors - structural abnormalities, medications, metabolic disturbances, neurological disorders, and other general conditions. Docusate is a stool softener that has been widely used, in combination with other stimulating laxatives, to prevent and treat constipation in palliative care patients. In the past decade there has been controversy about its effectiveness in these populations, but no controlled trials have been conducted on the use of docusate in palliative patients. The purpose of this study is to assess the effectiveness of docusate in preventing and treating constipation in palliative care patients. The study design is a randomized, double-blind, placebo-controlled trial to compare the current standard treatment (docusate in combination with a laxative, sennoside) to that of a sennoside laxative alone. A total of 70 patients (35 in each group) will be recruited from the Palliative Care Unit at St. Joseph's Auxiliary Care Hospital, the Mel Miller Hospice at the Edmonton General Continuing Care Hospital, and CapitalCare Norwood in Edmonton, Alberta, Canada. Patients must be ≥ 18 years of age, able to take oral medication, without difficulty swallowing, have a palliative performance ≥ 20%, and do not have a stoma. The duration of treatment will be for 10 days. The main outcome measures will include bowel frequency, stool consistency, other interventions (suppositories, enemas), difficulty defecating, and sense of inability to evacuate completely. This study will provide insight into the effectiveness of docusate in preventing and treating constipation in palliative patients who are cared for by family physicians and specialized palliative care providers. If docusate is found to have no added benefit,it has the potential to enhance the quality of life for palliative care patients by reducing the number of medications taken and reducing the palliative care team's (e.g. nursing) workload and cost.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • greater than or equal to 18 years of age
  • new admissions
  • able to take oral medications
  • patient and/or personal directive agent (proxy) provides written consent
  • does not have a stoma
  • no difficulty swallowing
  • no previous intolerance/contraindications to docusate
  • palliative performance greater than or equal to 20%

Exclusion criteria

  • less than 18 years of age
  • failing to provide consent
  • unable to take oral medication/difficulty swallowing
  • previous intolerance/contraindications to docusate (Colace)
  • patients who have a stoma
  • palliative performance status < 20%

Treatment and study plan

Docusate Sodium, Sennoside

Drug

Docusate sodium: given in capsule form (100 mg/capsule), at a dosage of 200 mg, taken twice daily for 10 days.

Sennoside: will be given in tablet form (8.6 mg), 1-3 tablets taken 1-3 times daily for 10 days.

Other names: Colace, Senokot

Sennoside + Placebo

Drug

Sennoside: will be given in tablet form (8.6 mg), 1-3 tablets taken 1-3 times daily for 10 days.

Placebo: will be taken in capsule form, similar in size, shape, and color to docusate, taken twice daily for 10 days

Other names: Senokot

Primary outcomes

  1. Stool Frequency

    Time frame: 10 days

  2. Stool Consistency

    Time frame: 10 day

  3. Difficulty Defecating

    Time frame: 10 day

  4. Symptoms Related to Constipation (pain, nausea, appetite loss, abdominal discomfort, shortness of breath)

    Time frame: 10 day

  5. Type of Additional Bowel Care Interventions which may be Required

    Time frame: 10 days

Sponsors and collaborators

Lead sponsor

University of Alberta

Other

Collaborators

  • Capital Care
  • College of Family Physicians of Canada
  • Covenant Health, Canada

Registry information

Official study title

Randomized, Double-Blind, Placebo-Controlled Trial of Oral Docusate for Preventing/Treating Constipation in Palliative Care Patients.

Important dates

Study start
2006
Primary completion
2010
Study completion
2010
First posted
May 14, 2009
Registry last updated
Apr 20, 2011

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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