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Prevention of constipation during treatment with opioids: magnesiumoxide versus macrogol/elektrolytes

Prevention of constipation during treatment with opioids: magnesiumoxide versus macrogol/elektrolytes

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2007-007610-10-NL
Enrollment
Unknown
Registered
2008-08-13
Start date
2009-01-13
Completion date
Unknown
Last updated
2012-03-19

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

Conditions

Palliative care cancer patients starting with opioids MedDRA version: 9.1 Level: LLT Classification code 10010774 Term: Constipation

Interventions

Trade Name: Movicolon Product Name: . Pharmaceutical Form: Powder for oral suspension INN or Proposed INN: Kaliumchloride CAS Number: 7447-40-7 Concentration unit: mg milligram(s) Concentration type:

Sponsors

UMC Utrecht
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Palliative care cancer patients started on morphine, fentanyl, oxycocodon, hydromorphon, methadone, codeine or tramadol Age >18 years Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria: Patients with a contra-indication for laxatives Patiens who have used laxatives within four weeks prior to inclusion in the study Estimated life expectancy <3 months

Design outcomes

Primary

MeasureTime frame
Main Objective: To compare magnesiumoxide and Movicolon with regard to the prevention of constipation in palliative care cancer patients started on opioids;Secondary Objective: To compare magnesiumoxide and Movicolon with regard to side effects and patient preference in palliative care cancer patients started on opioids;Primary end point(s): Level of constipation (as assessed by the PAC SYM, a constipation symptom assessment instrument)

Countries

Netherlands

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026