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A randomized, open clinical trial to compare the effects of conventional care and conventional care combined with palliative care on the symptoms and quality of life of patients who had diagnosed with therioma

A randomized, open clinical trial to compare the effects of conventional care and conventional care combined with palliative care on the symptoms and quality of life of patients who had diagnosed with therioma

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-16008521
Enrollment
Unknown
Registered
2016-05-23
Start date
2016-05-24
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Cancer patients

Interventions

Control group:routine intervention measures only
Experimental group:routine intervention measures and palliative care

Sponsors

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Aged 18 years old and more; (2) Diagnosed with lung cancer, mammary cancer or gastrointestinal tumor by histology or cytology; (3) At least one physical / psychological symptom which is difficult to control; (4) Signed informed consent form; (5) ECOG physical condition is 0-3.

Exclusion criteria

Exclusion criteria: (1) Participants with mental disease history or psychiatric history or being lunatic; (2) With no legal capacity / limited capacity; (3) With medical or psychological conditions which impede the participants to complete the study or to sign the informed consent form; (4) Central nervous system damage and consciousness disorder that caused by any disease; (5) The level of peripheral nervous disease >=2 or hearing disability; (6) With alcohol and ( or ) drug abuse; (7) Investigator believed that the subjects who had any of the medical conditions or diseases that may be harmful to the development of this study.

Design outcomes

Primary

MeasureTime frame
The improvement of the subjects' physical / psychological symptoms;the improvement of the subjects' quality of life;

Secondary

MeasureTime frame
Total survival time;Average length of stay;

Countries

China

Contacts

Public ContactWen Qu

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

xhhlbzlzx@163.com+86 13971362616

Outcome results

None listed

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