Preoperative functional and breathing tests to predict early recovery after colorectal cancer surgery
The Effect of Functional Status and Respiratory Parameters on Early Postoperative Clinical Outcomes in Patients With Colorectal Cancer
We will see if simple preoperative functional and breathing tests can predict early recovery and complications for adults having colorectal cancer surgery.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 42 (estimated) |
| Ages | 18 Years to 80 Years |
| Sex | All |
| Sponsor | Inonu University Academic / other |
| Locations | 1 site (Malatya) |
| Trial ID | NCT07529301 on ClinicalTrials.gov |
What this trial studies
This is an observational cohort that measures patients' functional status and respiratory parameters before colorectal cancer surgery and follows them daily from the first postoperative day until discharge. Researchers will record early outcomes such as postoperative pulmonary complications, overall complication rates, length of hospital stay, and early mortality. The study excludes people with musculoskeletal or cognitive conditions that prevent completion of the tests and those with prior major surgery. It is conducted at a single center (İnönü University Turgut Özal Medical Center in Malatya, Turkey).
Who should consider this trial
Good fit: Adults aged 18–80 scheduled for elective colorectal cancer surgery who can complete functional and respiratory tests and provide informed consent.
Not a fit: Patients with musculoskeletal limitations, mental impairment, psychiatric disorders, or a history of prior major surgery who cannot complete the required assessments are unlikely to benefit from this study's approach.
Why it matters
Potential benefit: If successful, the findings could help clinicians identify higher-risk patients before surgery so they can offer targeted breathing training or physical preparation to reduce complications and shorten hospital stays.
How similar studies have performed: Previous studies have linked poor functional and respiratory measures with higher postoperative complications, so this approach is supported by existing evidence though results vary by setting.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria Being between 18 and 80 years of age Voluntary agreement to participate in the study Exclusion Criteria Withdrawal from the study at the participant's own request Elimination Criteria Presence of a musculoskeletal condition that may prevent completion of the planned assessments Presence of a mental impairment History of psychiatric disorder History of previous major surgery
Where this trial is running
Malatya
- İnönü University Turgut Özal Medical Center General Surgery Polyclinic — Malatya, Turkey (Türkiye) (Recruiting)
Study contacts
- Study coordinator: Müşerref Ebru YALÇIN
- Email: M.ebrusen@gmail.com
- Phone: +90 555 713 6666
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.