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Effects of postoperative pain, constipation, and anxiety in patients with mixed hemorrhoids: A randomized controlled trial

Effects of postoperative pain, constipation, and anxiety in patients with mixed hemorrhoids: A randomized controlled trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR1900002268
Enrollment
Unknown
Registered
2019-04-05
Start date
2019-05-02
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

Sponsors

Shanghai Municipal Hospital of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) patients who met the criteria for diagnosis of mixed hemorrhoids in the guidelines for clinical diagnosis and treatment of hemorrhoids (2006 edition) and underwent external stripping and internal ligation (hemorrhoidectomy for stage III to IV hemorrhoids); (2) aged 18 to 65 years; (3) anus with normal structure and function; (4) the patient conscious, cultural level can normal communication with medical staff to normal; (5) able to cooperate with medical staff to successfully complete the visual analogue scale of pain score; (6) patients signed the informed consent.

Exclusion criteria

Exclusion criteria: (1) pregnant or lactating woman; (2) patients with severe circulatory system, nervous system, urinary system, digestive system, hematopoietic system and other diseases, and patients with psychological disorders; (3) patients with other anorectal diseases, such as ulcerative rectal disease, malignant tumor, and severe anal infection; (4) patients who have a history of drug abuse or painkiller abuse, or who received drug analgesia 10 hours before surgery; (5) severe complications, severe allergic reactions, or serious adverse events; (6) patients participating in clinical trials of other drugs; (7) find out parts of the skin is not suitable for the operator.

Design outcomes

Primary

MeasureTime frame
Pain;constipation;

Secondary

MeasureTime frame
Anxiety score;

Countries

China

Contacts

Public ContactWang Xian

Shanghai Municipal Hospital of Traditional Chinese Medicine,Shanghai University of Traditional Chinese Medicine

0560@szy.sh.cn+86 13651925493

Outcome results

None listed

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