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TIVA Versus Balanced Anesthesia on Muscle Mass in CRC Surgery

Total Intravenous Anesthesia Versus Balanced Anesthesia on Loss of Muscle Mass After Colorectal Cancer Surgery

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07237438
Acronym
TIVABAL-CRC
Enrollment
40
Registered
2025-11-19
Start date
2025-09-20
Completion date
2026-06-30
Last updated
2025-11-19

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

Conditions

Colorectal Cancer (CRC), Sarcopenia

Keywords

colorectal cancer, sarcopenia, ultrasound, bioimpedance

Brief summary

This study is aimed at clarifying changes in body composition during the perioperative period and identifying risk factors for skeletal muscle mass loss in patients with colorectal cancer. The investigators will asess the impact of the type of anaesthesia (total intravenous anaesthesia/sevoflurane anaesthesia) for colorectal surgery on the muscle function and mass, which will be evaluated using ultrasound, dynamometry and bioimpedance.

Interventions

evaluate the impact of the type of anaesthesia (total intravenous anaesthesia (TIVA)/sevoflurane anaesthesia) for colorectal surgery on the muscle function and mass

PROCEDUREsevoflurane anaesthesia

evaluate the impact of the type of anaesthesia (total intravenous anaesthesia (TIVA)/sevoflurane anaesthesia) for colorectal surgery on the muscle function and mass

Sponsors

Regional Institute of Oncology, Iasi, Romania
CollaboratorUNKNOWN
Grigore T. Popa University of Medicine and Pharmacy
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

• adult patients diagnosed with colorectal cancer and scheduled for open colorectal surgery at the Regional Institute of Oncology, Iaşi, Romania

Exclusion criteria

* lack the capacity to consent * extremity amputation * paraplegia * diseases affecting the muscles (such as stroke, lower-limb immobilization from a plaster, neurodegenerative diseases, peripheral neuropathy or muscle dystrophy) * terminal cancer

Design outcomes

Primary

MeasureTime frameDescription
Ultrasonographic assessment of muscle massFrom enrollment to 5 days after surgeryUltrasonographic muscle assessment is standardised in the assessment of muscle according to the SARCUS (Sarcopenia through UltraSound) working group recommendations. Rectus femoris muscle will be evaluated at 50% distance between the anterior superior iliac spine and the superior pole of the patella, in a lying position with knees in 10°, for muscle thickness and muscle cross-sectional area (CSA). Three measurements will be taken for each data point, and the average value will be used for further analysis. The biceps brachii muscle will be evaluated at 50% distance acromioclavicular joint and the elbow crease, in a supine position. Muscle thickness can be easily defined as the maximal vertical distance between the superficial and deep fasciae.
Muscle function assessmentFrom enrollment to 5 days after surgeryMeasuring grip strength is simple and inexpensive. Grip strength will be determined bilaterally. Each measurement will be performed three times on the left and right extremities with 20 seconds intervals between the measurements. The maximum measured value in kilograms will be used for analysis.
Bioimpedance assessment of lean and fat tissue massFrom enrollment to 5 days after surgeryThe bioimpedance measurements will be performed by a trained operator according to the manufacturer's recommendations. The Body Composition Monitor provides a quantitative measure of lean tissue and fat tissue mass. In contrast to earlier bioimpedance methodologies, the bioimpedance spectroscopy expresses body composition as a three-compartment model, providing overhydration, lean tissue index (LTI), and fat tissue index (FTI), whereby LTI and FTI are the respective tissue masses normalized to height squared.

Secondary

MeasureTime frame
Hospital length of stayFrom enrollment to the patient discharge, up to 52 weeks
Mortality28 and 90-day mortality after surgery

Other

MeasureTime frameDescription
CorrelationFrom enrollment to 5 days after surgeryCorrelation between muscle strength and muscle mass using dynamometry and echography and bioimpedance at different time points

Countries

Romania

Contacts

Primary ContactIanis Siriopol
ianis.siriopol@gmail.com+40 746215 967

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026