Perioperative Assessment of Physical Capacity in Elderly Patients Undergoing Laparoscopic Colorectal Surgery
Perioperative Assessment of Physical Capacity in Elderly Patients Undergoing Laparoscopic Colorectal Surgery- Atlas Study
Evaluation of preoperative physical capacity and its evolution in the postoperative period in older patients after undergoing laparoscopic surgery for colorectal cancer, with the test:
- Short Physical Performance Battery (SPPB)
After the inclusion of the first 10 patients, a preliminary feasibility study will be carried out and thus we have coverage of this pilot study.
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Study Type
Study Type
Enrollment (Anticipated)
Enrollment
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients age ≥65 years.
- ASA I-III
- Patients with absence of cognitive deficit.
- Informed consent signed prior to surgery.
Exclusion Criteria:
- Refusal of the patient to participate in the study.
- Patients with disabilities to give their consent.
- ASA IV-V.
- Pregnancy or lactation.
- Health status that prevent physical exercise, such as unstable heart disease, severe systematic disease, or serious orthopedic conditions
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Evaluation of the physical capacity
Time Frame: 21 days before surgery
|
Evaluation of the physical capacity only with the Short Physical Performance Battery (SPPB) questionnaire
|
21 days before surgery
|
|
Evaluation of the physical capacity
Time Frame: 21 days after surgery
|
Evaluation of the physical capacity only with the Short Physical Performance
|
21 days after surgery
|
Collaborators and Investigators
Sponsor
Sponsor
Study record dates
Study Major Dates
Study Start (Anticipated)
Study Start
Primary Completion (Anticipated)
Primary Completion
Study Completion (Anticipated)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
Other Study ID Numbers
- ATLAS
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Colorectal Disorders
-
NCT00868400CompletedColorectal Disorders | Colorectal Surgery
-
NCT04704817Not yet recruitingColorectal Disorders
-
NCT04461054Unknown
-
NCT03131180CompletedColorectal Disorders
-
NCT05262296Completed
-
NCT03985111CompletedColorectal Disorders
Clinical Trials on Perioperative assessment of physical capacity
-
NCT06563154Completed
-
NCT02431156Unknown
-
NCT04591067CompletedJoint Diseases | Musculoskeletal Diseases | Hip Dysplasia
-
NCT04753346Recruiting
-
NCT03638050UnknownAcute Myocardial Infarction | Six-minute Walk Test
-
NCT07509372CompletedPostoperative Cognitive Dysfunction | Delirium, Postoperative
-
NCT05188755CompletedLymphoma, Non-Hodgkin | Hodgkin Disease | Young Adults
-
NCT07343388CompletedPostoperative Pain | Preoperative Anxiety | Urogenital Diseases | Emergence Delirium in Pediatric Anesthesia
-
NCT04031924CompletedLiver Transplant Disorder