Skip to content

A study to compare the efficiency of sterile talc, tetracycline and bleomycin as sclerosing agents for medical pleurodesis in the treatment of malignant pleural effusions

A study to compare the efficiency of sterile talc, tetracycline and bleomycin as sclerosing agents for medical pleurodesis in the treatment of malignant pleural effusions

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN35591640
Enrollment
Unknown
Registered
2003-09-12
Start date
2001-06-01
Completion date
Unknown
Last updated
2016-10-17

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

Conditions

Malignant pleural effusion Cancer Malignant neoplasm without specification of site

Interventions

Randomised controlled trial. Random allocation to: 1. Sterile talc 2. Tetracycline 3. Bleomycin

Sponsors

Department of Health (UK)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Predominantly lung cancer patients with a selection of other cancer patients with malignancy effusions. (This is likely to be mostly breast cancer patients.)

Exclusion criteria

Exclusion criteria: Not provided at time of registration

Design outcomes

Primary

MeasureTime frame
This study should provide information as to which of these most commonly used agents for medical pleurodesis is most effective in preventing further malignant pleural effusions. It should provide information on which agent if any is associated with more prolonged survival. It should provide information on issues such as pain and infection rates during pleurodesis with these agents. Hopefully, these data will lead to an evidence based choice of sclerosing agent for cancer patients with malignant pleural effusions.

Secondary

MeasureTime frame
Not provided at time of registration

Countries

United Kingdom

Outcome results

None listed

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