Low Central Venous Pressure with Milrinone During Lumbar Spine Surgery: a randomized controlled trial

Low Central Venous Pressure with Milrinone during Posterior Lumbar Spinal Fusion: a randomized controlled trial

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR1900022610

Enrollment

Unknown

Registered

2019-04-18

Start date

2019-05-01

Completion date

Unknown

Last updated

2019-04-23

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

Conditions

Intraoperative bleeding

Interventions

experimental group :Milrinone is continuously pumped during operation

control group:sodium chloride injection

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Fitting line of spinal fusion surgery, ASA class for I - III, aged 18 to 80 years.

Exclusion criteria

Exclusion criteria: Revision surgery; previous history of coagulation dysfunction; Non-jackson table operating table was used; subjects who are unwilling to participate in the clinical trial; Subjects with severe cardiovascular and cerebrovascular diseases and liver and kidney dysfunction; recently (within 2 weeks) using heparin antithrombin or warfarin anticoagulant factor or aspirin antiplatelet aggregation and other anticoagulant drugs.

Design outcomes

Primary

Measure	Time frame
Intraoperative blood loss;Autologous blood transfusion;Allogeneic blood transfusion;	—

Secondary

Measure	Time frame
Operators' evaluation of the surgical environment and ease of operability;Days for hospitalization;	—

Countries

China

Contacts

Public ContactShaoxiao Sun

Huadong Hospital Affliated to Fudan University

sunshaoxiao@me.com+86 13501882382

Outcome results

None listed

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