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Urine Retention Rate Between Spinal and General Anesthesia for Anorectal Surgery

Pain Score and Urine Retention Rate Between Spinal and General Anesthesia for Anorectal Surgery, Retrospective Observation Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05571202
Enrollment
1400
Registered
2022-10-07
Start date
2017-01-01
Completion date
2022-09-30
Last updated
2023-01-31

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

Conditions

Anorectal Disorder

Keywords

anorectal surgery, hemorrhoid, anesthesia

Brief summary

Anorectal surgery includes pilonidal sinus, hemorrhoidectomy, anal fissure, and anal fistula operations. General and spinal anesthesia were common anesthetic methods in anorectal surgery. We designed this study to test the hypothesis that general anesthesia was superior than spinal anesthesia with respect to urine retention rate, pain score, recovery time, and side effects.

Detailed description

Anorectal surgery includes pilonidal sinus, hemorrhoidectomy, anal fissure, and anal fistula operations. Deep level of anesthesia is required for these surgeries. Excellent operation conditions and rapid recovery is anticipated for optimal anesthesia. Various surgical and anesthetic techniques, including spinal anesthesia, general anesthesia and local infiltration have been used to increase the level of patients' perioperative analgesia and decrease the length of stay in the hospital. Among them, general and spinal anesthesia were common anesthetic methods in anorectal surgery. We designed this study to test the hypothesis that general anesthesia was superior than spinal anesthesia with respect to urine retention rate, pain score, recovery time, and side effects. Inclusion Criteria: * \>20 years old patients * ASA 1-2 patients * Patients who will undergo anorectal surgery with including hemorrhoidectomy, fistulectomy, fistulotomy, fissurectomy and anoplasty. Exclusion Criteria: * Having known hypersensitivity to amide type local anesthetics * Patients ASA \>=3 * Surgery methods: hemorrhoidopexy, Laser hemorrhoidoplasty * Fournier gangrene patients * Surgery due to previous complications. Characteristic data 1. Age, Gender, ASA class, 2. Past history: medical history, surgical history 3. Previous anorectal history 4. Type of anorectal surgery, number of hemorrhoidectomy 5. Methods of anesthesia, posture during surgery 6. Postoperative recovery room record: vital sign, Post Anaesthetic Discharge Scoring System (0-10, \>9 can discharge) 7. Ward record: vital sign and urine retention need foley catherization

Interventions

PROCEDUREGeneral anesthesia plus local infiltration

The eligible patients underwent anorectal surgery under general anesthesia (GE, GM, IVG) plus locally injected analgesics.

PROCEDURESpinal anesthesia

The eligible patients underwent anorectal surgery under spinal anesthesia alone.

Sponsors

Taichung Veterans General Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* \>20 years old patients * ASA 1-2 patients * Patients who will undergo anorectal surgery with including hemorrhoidectomy, fistulectomy, fistulotomy, fissurectomy and anoplasty.

Exclusion criteria

* Having known hypersensitivity to amide type local anesthetics * Patients ASA \>=3 * Surgery methods: hemorrhoidopexy, Laser hemorrhoidoplasty * Fournier gangrene patients * Surgery due to previous complications

Design outcomes

Primary

MeasureTime frameDescription
Urine retention rate0-24 hours post operation.urine retention events needs foley catheterization
Pain score0-24 hours post operation.Visual Analogue Scale (VAS)

Secondary

MeasureTime frameDescription
surgery complications0-30 days post operative days.surgery complications
anesthesia complications0-30 days post operative days.anesthesia complications rate

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026