Impact of early mobilisation on the day of the surgery on patients with a primary total hip replacement

Impact of early mobilisation on the day of the surgery on patients with a primary total hip replacement - FAST_HIP_KLH

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00017096

Enrollment

180

Registered

2019-07-12

Start date

2019-07-15

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

M16.9

Interventions

Group 1: Patients will be mobilized on the day of the surgery approximately 4 hours after surgery. Group 2: Patients will be mobilized one day after the day of surgery.

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Implantation of a primary total hip replacement, alt least 18 years of age, Patient information orally and in writing, written consent

Exclusion criteria

Exclusion criteria: Primary exclusion criteria: Planned use of surgical drain or additional surgical procedures that do not allow day-of-surgery mobilization. Secondary exclusion criteria: Occurrence of complications or unplanned use of drain or the occurence of complications that do not allow day-of-surgery mobilization.

Design outcomes

Primary

Measure	Time frame
Time interval between surgery and readiness for discharge.	—

Secondary

Measure	Time frame
1. pain intensity (will be recorded independently from the study by the staff nurses according to hospital standard). 2. analgesic intake (will be recorded independently from the study by the staff nurses according to hospital standard). 3. mobility (will be recorded independently from the study by the staff physiotherapists according to hospital standard). 4. complications (will be recorded independently from the study by the staff physician according to hospital standard).	—

Measure

Time frame

1. pain intensity (will be recorded independently from the study by the staff nurses according to hospital standard). 2. analgesic intake (will be recorded independently from the study by the staff nurses according to hospital standard). 3. mobility (will be recorded independently from the study by the staff physiotherapists according to hospital standard). 4. complications (will be recorded independently from the study by the staff physician according to hospital standard).

—

Countries

Germany

Contacts

Public ContactAxel Jakuscheit

Orthopädische Klinik König-Ludwig-Haus

a-jakuscheit.klh@uni-wuerzburg.de0049 931 803 0

Outcome results

None listed

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