Clinical efficacy of enhanced recovery after surgery protocol in patients undergoing robotic assisted laparoscopic prostatectomy

The construction and implementation of a multidisciplinary precision rehabilitation model for prostate cancer surgery patients based on a smart medical platform evidence research

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100047730

Enrollment

Unknown

Registered

2021-06-24

Start date

2017-08-01

Completion date

Unknown

Last updated

2022-02-28

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

Conditions

prostate cancer

Interventions

control group:routine nursing measures

ERAS group:enhanced recovery after surgery protocol

Eligibility

Sex/Gender

Male

Inclusion criteria

Inclusion criteria: Patients were aged 18 to 85 years, in good physical condition, with prostate cancer confirmed by preoperative prostate tissue biopsy. All patients had treated with RALP

Exclusion criteria

Exclusion criteria: emergency surgery; severe cardiovascular disease, pulmonary dysfunction, severe hemorrhagic tendency, or blood clotting disorders that significantly increased surgical risk; body mass index (BMI) >30 kg/m2 or patients with 3 points nutritional score according to NRS2002, and those with no written consent were excluded.

Design outcomes

Primary

Measure	Time frame
length of hospital stay;POD 1 drainage;POD 1 Alb;POD 1 Hb;first defecation;first ambulation;first intake of clear liquid;time to liquid;	—

Secondary

Measure	Time frame
operative time;blood loss;	—

Countries

China

Contacts

Public ContactCao Jie

Changhai Hospital, First Affiliated Hospital of Naval Medical University

celion2004@126.com+86 13817797641

Outcome results

None listed

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