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A clinical trial on the effect of critical pathway method in Colorectal cancer Patients

A clinical trial on the effect of critical pathway method in comparison with routine on length of stay, complication of surgery and patient satisfaction from nursing care in patients with Colorectal cancer.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013073014225N1
Enrollment
70
Registered
2014-08-29
Start date
2013-08-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Colorectal cancer disease. Colon disease,unspecified

Interventions

Intervention 1: The intervention is implementing the critical path, that all patient interventions, including tests, diet, patient education is defined in specific line time. At the end of interventio
Treatment - Drugs
The intervention is implementing the critical path, that all patient interventions, including tests, diet, patient education is defined in specific line time. At the end of intervention patient satisf
All interventions in control group performed with routin hospital.

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients with cancer is confirmed; colorectal cancer is not metastatic; Have the ability to speak in Farsi; Patient's age is between 20 to 70 years; Patient has not history of previous surgery on the colon or rectum; severe cognitive impairment or a history of mental illness is not visible; BMI less than 18 and not more than 35; Patient has not Other underlying chronic diseases such as diabetes, liver failure, kidney function; functional index score of at least 60; Patients are operated by a single surgeon; Patients has not Drug addiction of any kind. Exclusion criteria: any time a patient is not satisfied to continue research; Patients transferred to another hospital or discharge with personal satisfaction; Patient with Laparoscopic surgery; Patients who do not require Kolostomy or Ileostomy.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Patient satisfaction. Timepoint: The end of intervention. Method of measurement: Satisfaction questionair.;Complications after surgery. Timepoint: During the intervention. Method of measurement: Recorded from patient file.;Length of stay. Timepoint: End of intervention. Method of measurement: Record from patient file.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBahareh Abavi Torghabeh

Mashhad Faculty of Nursing and Midwifery

abavib901@mums.ac.ir+98 51 1859 1511

Outcome results

None listed

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