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Impact of Remote Ischemic Conditioning on Free Flaps

Impact of Remote Ischemic Conditioning on Free Flaps

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00025473
Enrollment
40
Registered
2022-02-14
Start date
2021-10-07
Completion date
Unknown
Last updated
2025-10-06

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

Conditions

Ischemia-reperfusion injury

Interventions

Group 1: Intervention group: RIC is performed by repetitively inflating and deflating a standard blood pressure cuff placed on the upper arm (three 10 min cuff inflations and deflations) one day preop

Sponsors

Universitätsklinikum Regensburg
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Free flap surgery

Exclusion criteria

Exclusion criteria: Children, patients with a health care proxy, contraindications for blood pressure cuff inflation (e.g. post-traumatic, vascular disease) or indocyanine-green fluorescence angiography (e.g. manifest hyperthyroidism, iodine allergy)

Design outcomes

Primary

MeasureTime frame
Primary outcome measure: The fractional weight of insufficiently perfused and resected flap tissue related to total flap weight is measured based on clinical examination and Indocyanine green fluorescence angiography according to the study center's clinical routine.

Secondary

MeasureTime frame
Secondary outcome measures: occurrence / severity of wound healing disturbances, revision surgery, other postoperative complications (e.g. fat necrosis, oil cysts). These parameters are assessed over a six week postoperative period via clinical examination, further non-invasive diagnostic measures (e.g. ultrasound) and photo documentation.

Countries

Germany

Contacts

Public ContactAlexandra Anker

Universitätsklinikum Regensburg

alexandra.anker@ukr.de0941 944 6763

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026