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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age45+
SponsorGeneral Hospital of Ningxia Medical University

About this trial

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.

Eligibility criteria

Qualifiers

Over 45 years old;

ASA Grade II - III;

BMI 18-35kg/㎡;

Agree to participate in this study and sign the informed consent form.

Disqualifiers

Those who refuse to participate in the experiment;

Those who suffer from language or hearing impairments and are unable to communicate;

Those with contraindications for sacral canal block.

Trial design

Treatments tested in this trial

  • Sacral canal block combined with general anesthesia
  • Simple general anesthesia

Treatment groups

80 Participants
are divided into 2 treatment groups