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Ischemic Preconditioning and Thiol-disulfide Balance

Effect of Ischemic Preconditioning on Dynamic Thiol-disulfide Balance, Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05082207
Enrollment
60
Registered
2021-10-18
Start date
2021-10-16
Completion date
2022-05-15
Last updated
2022-08-17

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

Conditions

Tourniquets

Keywords

thiol/disulfide homeostasis, ischemic preconditioning

Brief summary

Various strategies have been proposed to prevent or mitigate the effects of ischemia-reperfusion injury following the use of tourniquets in orthopedic surgery cases. One of them is applying remote ischemic preconditioning. This randomized controlled trial is planned to evaluate the effectiveness of remote ischemic preconditioning in preventing tourniquet-induced ischemia-reperfusion injury in total knee arthroscopy with dynamic thiol-disulfide homeostasis.

Interventions

OTHERRemote Ischemic Preconditioning

Three cycles of 5-min upper limb ischemia and 5-min reperfusion using a blood-pressure cuff inflated to a pressure of systolic blood pressure plus 50 mm Hg.

OTHERsham group

a deflated cuff placed on the upper arm for 30 min

Sponsors

Konya Meram State Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
Yes

Inclusion criteria

* ASA I-III patients who will undergo total knee arthroplasty surgery under elective conditions

Exclusion criteria

* emergency operation, * Underlying neurological disorder, * Underlying peripheral vascular disease, * other types of concurrent surgery.

Design outcomes

Primary

MeasureTime frameDescription
thiol/disulfide homeostasis24th hour after surgeryThiol/disulphide homeostasis will be determined at preoperatively and just before the tourniquet opened and at the 1st, 6th and 24th hours after the tourniquet is opened.

Countries

Turkey (Türkiye)

Outcome results

None listed

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