Prospective randomized controlled evaluation of the outcomes of two different postoperative therapeutic concepts for rotator cuff repair surgery

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00017519

Enrollment

Registered

2019-08-27

Start date

2014-12-01

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

M75.1

Interventions

Group 1: n=37 patients with a conservative therapy approach after rotator cuff repair surgery, where initially no movement therapy will be conducted Group 2: n=37 patients with a progressive therapy a

Eligibility

Sex/Gender

All

Age

18 Years to 100 Years

Inclusion criteria

Inclusion criteria: Patients with rotator cuff repair surgery

Exclusion criteria

Exclusion criteria: Not eligible for surgery Revision-Surgery Server osteoarthritis Preoperative frozen shoulder massive tear (> 5cm) wide tendon retraction massive atrophy

Design outcomes

Primary

Measure	Time frame
prevalence of reruptures 1 year postop	—

Secondary

Measure	Time frame
Range of motion, life quality, strength in the operated shoulder, pain level	—

Countries

Germany

Contacts

Public ContactLothar Seefried

Klinische StudieneinheitOrthopädische Klinik, Universität Würzburg

l-seefried.klh@uni-wuerzburg.de+49 931 803 3575

Outcome results

None listed

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