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A Randomized Controlled Study Comparing Ultra-Low Concentration Ropivacaine with Bupivacaine in Spinal Anesthesia for Promoting Early Ambulation After Anorectal Surgery: Analysis Based on Early Mobilization and Medical Safety

A Randomized Controlled Study Comparing Ultra-Low Concentration Ropivacaine with Bupivacaine in Spinal Anesthesia for Promoting Early Ambulation After Anorectal Surgery: Analysis Based on Early Mobilization and Medical Safety

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500108389
Enrollment
Unknown
Registered
2025-08-29
Start date
2025-09-01
Completion date
Unknown
Last updated
2025-09-01

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

Conditions

Anorectal diseases

Interventions

Observation group (Group R) :0.15% ropivacaine 7.5mg spinal anesthesia
Control group (Group B):0.15% bupivacaine 7.5mg spinal anesthesia

Sponsors

Taiyuan Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Patients who undergo elective proctological surgery; 2. Operation time< 1 hour; 3. Age 18~60 years old; 4. ASA grade I.~II.; 5.BMI<=30kg/m^2 .

Exclusion criteria

Exclusion criteria: 1. Those with contraindications to spinal anesthesia; 2. Those with a history of local anesthetic allergy; 3. Preoperative Bromage score >0 points; 4. Those who cannot cross the bed voluntarily before surgery (including leg disability, sequelae of cerebral infarction, non-cooperation, etc.); 5. Patient refuses to participate in the study.

Design outcomes

Primary

MeasureTime frame
Blood pressure;The anesthesia plane;SPO2;Heart rate;

Secondary

MeasureTime frame
Anesthesia time;The onset time and duration of sensory and motor blockade, the length of hospitalization and the cost of hospitalization were recorded;Physician assistant score for back pain after assisting patient with bed transfer or transporting patient;Adverse reactions during and after surgery;Amount of access;Operation time;

Countries

China

Contacts

Public ContactWang Shengcui

Taiyuan Central Hospital

449206481@qq.com+86 151 3514 0402

Outcome results

None listed

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