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NCT Number: NCT04448041

CRANE Feasibility Study: Nutritional Intervention for Patients Undergoing Cancer Surgery in Low- and Middle-Income Countries

Aims: The CRANE feasibility study (A mixed methods study of malnutrition and sustainable nutritional intervention for patients undergoing cancer surgery in low- and middle-income countries) aims to investigate the identification of pre-operative malnourishment, data collection methods and acceptability of a nutritional intervention for a future trial to improve outcomes after cancer surgery in low- and middle-income countries (LMICs).

1. To identify and validate the most relevant nutritional screening tool for patients in LMICs undergoing surgery for cancer; 2. To identify a low cost sustainable nutritional intervention for patients in LMICs undergoing surgery for cancer; 3. To establish the feasibility of delivering a randomised trial of a sustainable nutritional intervention for patients in LMICs undergoing surgery for cancer.

Design: A mixed-methods study comprising of qualitative work including focus groups and interviews, trial of data collection and validation to test feasibility in clinical practice

Participants: Patients undergoing elective surgery for suspected cancer in LMICs

Outcomes Work package (WP) 1: The primary deliverable is the identification of a relevant, pragmatic, and acceptable nutritional screening tool.

WP 2: The primary deliverable is the identification of a low-cost and sustainable nutritional intervention. Focus groups and interviews will be held with patients and clinicians to explore the sustainability, implementation and acceptability of screening and interventions.

WP 3: The primary outcome will be to determine feasibility and acceptability of trial design. A number of outcome assessments and data collection instruments will be evaluated for feasibility, including anthropometric parameters and patient outcomes (30-day mortality, major post-operative complications, length of hospital stay and quality of life). A final study design, analysis plan, and health economic plan will be developed.

Sample size: For this feasibility study, the investigators will conduct multidisciplinary focus groups and interviews, perform and validate malnutrition screening in 200 patients across four countries and record patient 30-day outcomes. This will also include the time taken to collect data on 200 eligible patients. This sample size has been informed from previous malnutrition data originating from a large prospective international multicentre observational cancer study (GlobalSurg 3).

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Cape Coast Teaching Hospital, Cape Coast, Ghana

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Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Hospitals in LMICs who undertake planned (elective) cancer surgery for cancer.
  • Patients over 18 years of age (or the age of majority for the country);
  • Patients undergoing planned (elective) surgery for cancer;
  • Patients undergoing surgery where the intent is either curative or palliative;
  • Patients must be able and willing to provide written informed consent (signature or a fingerprint).

Exclusion criteria

  • Children (below age of majority for the country);
  • Patients undergoing emergency surgery;
  • Any operative indication other than cancer;
  • Patients unable to provide written informed consent;

Treatment and study plan

Malnutrition screening

Other

Primary comparison: Prevalence of malnutrition and impact on 30-day outcomes in patients undergoing surgery for cancer

Primary outcomes

  1. Prevalence of malnutrition

    Time frame: Immediately prior to surgery

    Malnutrition as measured using validated screening tools

  2. 30-day mortality rate

    Time frame: 30 days from surgery

    Death within 30 days of surgical procedure

Secondary outcomes

  1. 30-day complication rate

    Time frame: 30 days from surgery

    Defined with by Clavien-Dindo grade III or IV

  2. Length of stay

    Time frame: 30 days from surgery

    Length of hospital admission

  3. Re-operation rate

    Time frame: 30 days from surgery

    Re-operation within 30 days of surgical procedure

  4. Quality of life following surgery (EQ-5D-5L / WHODAS questionnaire (36 item))

    Time frame: 30 days from surgery

    Short-term quality of life for patients following surgery

  5. Readmission rates

    Time frame: 30 days from surgery

    Readmission within 30 days of surgery

  6. Recruitment rate

    Time frame: Through study duration, up to one year

    Time taken to recruit 200 patients

Sponsors and collaborators

Lead sponsor

University of Edinburgh

Other

Registry information

Official study title

A Cluster Randomised Feasibility Study of a Sustainable Nutritional Intervention for Patients Undergoing Cancer Surgery in Low- and Middle-Income Countries

Acronym: CRANE

Important dates

Study start
2020
Primary completion
2021
Study completion
2021
First posted
Jun 25, 2020
Registry last updated
Jun 7, 2024

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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