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Effect of different postoperative management regimens on patients with ileostomy restoration in ERAS model: a multicenter prospective randomized controlled trial

Effect of different postoperative management regimens on patients with ileostomy restoration in ERAS model: a multicenter prospective randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300073284
Enrollment
Unknown
Registered
2023-07-06
Start date
2023-07-06
Completion date
Unknown
Last updated
2023-07-10

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

Conditions

Rectal Cancer

Interventions

Experimental group:Oral antibiotics were given 48h after surgery, and the amount of fluid rehydration on the first day after surgery was 20ml/kg, including electrolyte replacement.
Control group:Intravenous antibiotics were given 48h after surgery, and the amount of fluid rehydration on the first day after surgery was 30ml/kg, including electrolyte replacement.

Sponsors

Department of Gastrointestinal Surgery, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: ? Aged 18-80 years old; ? Prophylactic ileostomy; ? Successful completion of ileostomy restoration surgery; ? Voluntarily agree to participate in this researcher.

Exclusion criteria

Exclusion criteria: ? Those who cannot speak the language; ? Those who cannot correctly judge their own physical condition due to mental illness, consciousness disorder, intellectual deficiency, etc.; ? Those who are undergoing other research and treatment, or suffer from other major diseases at the same time, which interferes with the observation of the results of this study.

Design outcomes

Primary

MeasureTime frame
Time of first anal exhaust;Time of first anal defecation;First time out of bed activity;Score on the quality of Life scale QLQ-C30;

Secondary

MeasureTime frame
Score on the digital Assessment Scale of pain degree;Serological trauma indicators;

Countries

China

Contacts

Public ContactWang Xiaodong

Department of Gastrointestinal Surgery, West China Hospital of Sichuan University, Chengdu, Sichuan, China.

lockwan@qq.com+86 138 8226 7388

Outcome results

None listed

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