Actively Recruiting

Phase Not Applicable
Age: 45Years +
All Genders
Healthy Volunteers
NCT07064434

Sacral Canal Block for Hip Replacement the Efficacy and Safety of Controlled Intraoperative Hypotension

Led by General Hospital of Ningxia Medical University · Updated on 2025-07-14

80

Participants Needed

1

Research Sites

51 weeks

Total Duration

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AI-Summary

What this Trial Is About

To observe the efficacy and safety of sacral canal block in controlled blood pressure reduction during hip replacement in the elderly, and to provide a better option for controlled blood pressure reduction during clinical hip surgery.

CONDITIONS

Official Title

Sacral Canal Block for Hip Replacement the Efficacy and Safety of Controlled Intraoperative Hypotension

Who Can Participate

Age: 45Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age over 45 years
  • ASA Grade II to III
  • Body mass index between 18 and 35 kg/m²
  • Willingness to participate and sign informed consent
Not Eligible

You will not qualify if you...

  • Refusal to participate in the study
  • Language or hearing impairments that prevent communication
  • Contraindications to sacral canal block

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

General hospital of Ningxia medical university

Yinchuan, Ningxia, China

Actively Recruiting

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Research Team

X

Xinli Ni, MD

CONTACT

W

Wenxuan Ma

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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