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Effect of different TCM treatment schemes on postoperative complications of mixed hemorrhoids

Effect of different TCM treatment schemes on postoperative complications of mixed hemorrhoids

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200006354
Enrollment
Unknown
Registered
2022-07-09
Start date
2022-07-01
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

Mixed hemorrhoids

Interventions

Intervention group 1:Routine nursing + acupoint injection
control group:Routine nursing
Intervention group 3:Routine nursing + music therapy+acupoint injection
Intervention group 2:Routine nursing + music therapy

Sponsors

Deyang people's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Those who meet the diagnostic criteria of mixed hemorrhoids and voluntarily participate in the trial; (2) The operation of mixed hemorrhoids is external stripping and internal ligation, and the anesthesia method is spinal anesthesia; (3) Aged between 18-65 years, the patient gave informed consent and signed the informed consent form.

Exclusion criteria

Exclusion criteria: (1) For those who do not meet the diagnosis of mixed hemorrhoids, the operation method is not external stripping and internal ligation; (2) Patients with other intestinal diseases such as anal fistula, anal fissure, inflammatory bowel disease or intestinal malignant tumor, patients with serious diseases of heart, brain, kidney, urinary system, patients with mental diseases and coagulation dysfunction; (3) Patients with diabetes, infectious diseases and other diseases that affect wound healing; (4) Age 65 years old; (5) Those with hearing impairment, those without independent behavior ability and those with communication ability impairment; (6) Pregnant and lactating women; (7) Postoperative analgesia pump; (8) Patients with neostigmine specific contraindications; (9) Poor compliance, poor possibility of follow-up and unwilling to participate in the trial.

Design outcomes

Primary

MeasureTime frame
Defecation;Pain score;Postoperative urination;Incision edema;Wound healing time;

Countries

China

Contacts

Public ContactHuang Qin

Deyang people's Hospital

865170715@qq.com15181063296

Outcome results

None listed

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