NCT07352826

Brief Summary

Carbon monoxide (CO) is a colorless, odorless, and tasteless gas that exerts diverse biological effects across tissues and organs. At high concentrations, it is recognized as toxic because of harmful effects such as tissue hypoxia, oxidative stress, peroxynitrite formation, inflammation, apoptosis, and immune damage. However, the endogenous production of CO suggests that it may confer protective mechanisms to the host. These protective effects include inhibition of platelet activation, smooth muscle relaxation, vasoactive properties, anti-inflammatory and anti-apoptotic actions, and beneficial influences on neurotransmission. Despite its toxic potential, low-concentration endogenous CO may provide protection linked to the body's defense mechanisms. In this study, we aimed to investigate the anti-apoptotic effects of carbon monoxide at low concentrations. To this end, the relationships between COHb levels and plasma levels of NF-κB, NRF2, and PGC-1α were analyzed statistically.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
120

participants targeted

Target at P50-P75 for not_applicable

Timeline
3mo left

Started Feb 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress40%
Feb 2026Aug 2026

First Submitted

Initial submission to the registry

September 15, 2025

Completed
4 months until next milestone

First Posted

Study publicly available on registry

January 20, 2026

Completed
1 month until next milestone

Study Start

First participant enrolled

February 20, 2026

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 31, 2026

Expected
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 31, 2026

Last Updated

January 20, 2026

Status Verified

January 1, 2026

Enrollment Period

3 months

First QC Date

September 15, 2025

Last Update Submit

January 13, 2026

Conditions

Keywords

low flow anesthesiaCOHbNF-kBNRF2PGC-1 alpha

Outcome Measures

Primary Outcomes (4)

  • Blood COHb, NF-kB, NRF2, and PGC-1α levels during Low-Flow and Normal-Flow Anesthesia

    COHb concentrations

    24 HOUR

  • Blood COHb, NF-kB, NRF2, and PGC-1α levels during Low-Flow and Normal-Flow Anesthesia

    NF-kB concentrations

    24 HOUR

  • Blood COHb, NF-kB, NRF2, and PGC-1α levels during Low-Flow and Normal-Flow Anesthesi

    NRF2 concentrations

    24 HOUR

  • Blood COHb, NF-kB, NRF2, and PGC-1α levels during Low-Flow and Normal-Flow Anesthesi

    PGC-1α concentrations

    24 HOUR

Study Arms (4)

COHb

EXPERIMENTAL
Behavioral: low-flow anasthesiaBehavioral: Normal akımlı anestezi

TAS

EXPERIMENTAL
Behavioral: low-flow anasthesiaBehavioral: Normal akımlı anestezi

TOS

EXPERIMENTAL
Behavioral: low-flow anasthesiaBehavioral: Normal akımlı anestezi

HIF 1a

EXPERIMENTAL
Behavioral: low-flow anasthesiaBehavioral: Normal akımlı anestezi

Interventions

In Group LF, FGF will then be maintained at 0.6 L/min (O₂ 50%, air 50%), with desflurane adjusted to maintain MAC = 1

COHbHIF 1aTASTOS

In Group NF, FGF will be maintained at 2 L/min (O₂ 50%, air 50%) with desflurane adjusted to maintain MAC = 1..

COHbHIF 1aTASTOS

Eligibility Criteria

Age18 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • aged 18-70 years
  • classified as ASA I
  • scheduled for inhalational anesthesia lasting ≥2 hours

You may not qualify if:

  • Patients with cardiovascular disease, respiratory system disease, hepatic or renal disease
  • pregnant or breastfeeding women
  • trauma patients
  • those undergoing emergency surgery
  • procedures lasting \<2 hours
  • those receiving intraoperative blood transfusion
  • smokers
  • individuals who decline participation

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Veysel

Erzurum, Turkey (Türkiye)

RECRUITING

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, CARE PROVIDER
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

September 15, 2025

First Posted

January 20, 2026

Study Start

February 20, 2026

Primary Completion (Estimated)

May 31, 2026

Study Completion (Estimated)

August 31, 2026

Last Updated

January 20, 2026

Record last verified: 2026-01

Locations