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Oral B-Complex Vitamin (B6, B9 and B12) Prevents Low Anterior Resection Syndrome in Rectal Cancer Patients With Hyperhomocysteinemia

2026년 11월 4일 업데이트: Qilu Hospital of Shandong University

Oral B-Complex Vitamin (B6, B9 and B12) Supplementation for the Prevention of Low Anterior Resection Syndrome After Sphincter-Preserving Surgery in Rectal Cancer Patients With Hyperhomocysteinemia: A Randomized Controlled Trial

The goal of this clinical trial is to investigate if taking Oral B-Complex Vitamin (B6, B9 and B12) can help prevent low anterior resection syndrome (LARS) in rectal cancer patients with hyperhomocysteinemia after sphincter-preserving surgery for rectal cancer. LARS is a group of bowel problems that can occur after rectal cancer surgery, including frequent bowel movements, an urgent need to have a bowel movement, constipation, and loss of bowel control.

Our previous research suggests that hyperhomocysteinemia increased the occurrence of LARS. Folic acid, vitamin B6 and vitamin B12 are a safe, widely used way to treat hyperhomocysteinemia.

The main questions this study aims to answer are:

  • Does taking Oral B-Complex Vitamin (B6, B9 and B12) lower the rate of LARS 6 months after surgery?
  • How does this treatment affect internal anal sphincter (IAS) function?

Researchers will compare Oral B-Complex Vitamin (B6, B9 and B12) with a placebo (a look-alike tablet that contains no vitamins) to see if Oral B-Complex Vitamin (B6, B9 and B12) can help prevent LARS.

Participants will:

  • Take B-Complex Vitamin (B6, B9 and B12) every day for 6 months
  • Visit the clinic twice ( 3 months and 6 months after surgery) for checkups and tests
  • Complete the LARS score questionnaire 6 months after surgery

연구 개요

상세 설명

Low anterior resection syndrome (LARS) is a cluster of bowel dysfunction symptoms after sphincter-preserving surgery for rectal cancer, including incontinence, urgency, and frequent bowel movements. The Chinese Expert Consensus on the Diagnosis and Treatment of LARS (2025 edition) reports an incidence of 69.8% at 3 months and 62.3% at 6-9 months after low anterior resection. LARS may persist for years and substantially impair quality of life. LARS is multifactorial, involving reduced rectal capacity and compliance, internal anal sphincter dysfunction and nerve injury. No drug or treatment is currently available to prevent LARS.

Hyperhomocysteinemia (HHcy) is defined as a serum homocysteine (Hcy) level above 15 μmol/L. The pooled prevalence of hyperhomocysteinemia (Hcy >15 μmol/L) in China was 25.9%. The prevalence of hyperhomocysteinemia is higher in cancer patients. Hyperhomocysteinemia increases the risk of various cardiovascular and cerebrovascular diseases, including coronary heart disease and stroke.

Our preliminary data showed that, in a single-center cohort of 530 patients who underwent low anterior resection for rectal cancer at Qilu Hospital of Shandong University between December 2023 and December 2025, hyperhomocysteinemia was present in 105 of 205 patients with LARS (51.2%) and in 95 of 325 patients without LARS (29.2%). This suggests hyperhomocysteinemia may be a risk factor of LARS.

In a Sprague-Dawley rat model of low anterior resection, hyperhomocysteinemia shortened colonic transit time and increased fecal water content. Postoperative supplementation with folic acid, vitamin B6 and vitamin B12 lowered serum Hcy and reversed these changes.

In our prospective single-arm pilot study, 80 patients who met the same eligibility criteria received Oral B-Complex Vitamin treatment. No adverse events were observed. After 6 months, majority of patients' Hcy levels returned to normal. LARS occurrence was much lower than 62.3%.

연구 유형

중재적

등록 (추정된)

277

단계

  • 해당 없음

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 연락처 백업

  • 이름: Hao Wu, MD, PhD
  • 전화번호: +86 18560086947

연구 장소

    • Shandong
      • Jinan, Shandong, 중국, 250012
        • Qilu Hospital of Shandong University

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

Inclusion Criteria:

  • Aged 18 to 75 years
  • Body mass index (BMI) of 18.5 to 28 kg/m2
  • Low anterior resection performed for rectal cancer
  • Serum homocysteine level between 15 and 50 μmol/L both before and after surgery
  • No evidence of tumor recurrence or distant metastasis
  • No short-term postoperative complications at the time of enrollment
  • Able to resume oral intake after surgery
  • Signed written informed consent

Exclusion Criteria:

  • History of, or planned, neoadjuvant or adjuvant radiotherapy or chemotherapy
  • Other severe chronic diseases, such as cardiovascular or cerebrovascular disease, diabetes mellitus or chronic respiratory disease
  • Renal insufficiency, epilepsy, or other gastrointestinal diseases
  • Hyperhomocysteinemia caused by inherited defects, such as cystathionine beta-synthase deficiency, methylenetetrahydrofolate reductase (MTHFR) deficiency or hereditary folate malabsorption, screened by detailed medical and family history; highly suspected cases will be referred for specialist diagnosis and excluded
  • Participation in any other clinical study within the past 3 months

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 방지
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 네 배로

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Oral B-Complex Vitamin (B6, B9 and B12)

Participants will take Oral B-Complex Vitamin (B6, B9 and B12) tablets, one tablet orally twice daily, starting after resumption of oral intake following surgery. Serum homocysteine (Hcy) will be measured at 3 months after surgery: if Hcy remains above 15 μmol/L, the full dose will continue for another 3 months; if Hcy has returned to normal, the dose will be reduced to one tablet once daily.Treatment will continue until the 6-month postoperative visit.

Film-coated oral tablet (0.3 g) registered as a health food in China (filing No. G201937000905), manufactured by Dongying Guangyuan Biotechnology Co., Ltd. Each tablet contains vitamin B6 (pyridoxine hydrochloride) 1.38 mg, folic acid (vitamin B9) 286 μg and vitamin B12 (cyanocobalamin) 3.05 μg. Excipients include corn starch, maltodextrin, microcrystalline cellulose, silicon dioxide, magnesium stearate, calcium carbonate and a film-coating premix.

위약 비교기: Placebo

Participants will take placebo tablets identical in appearance, color, odor and packaging to the Oral B-Complex Vitamin (B6, B9 and B12) tablets, one tablet orally twice daily, starting after resumption of oral intake following surgery. The same homocysteine-based dose-adjustment rules as in the experimental arm will apply, and treatment will continue until the 6-month postoperative visit.

Oral placebo tablet (0.3 g) containing corn starch and maltodextrin, with no active vitamins, manufactured by Dongying Guangyuan Biotechnology Co., Ltd. under good manufacturing practice. The placebo tablets are identical in appearance, color, odor and packaging to the Oral B-Complex Vitamin (B6, B9 and B12) tablets.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Incidence of Low Anterior Resection Syndrome (LARS)
기간: 6 months after surgery (3 months after stoma closure for participants whose protective stoma has not been closed by 6 months after surgery)

Proportion of participants with LARS, defined as a total score of 21 or higher on the LARS score questionnaire. The LARS score is a validated 5-item questionnaire on bowel function (Emmertsen and Laurberg, 2012), with a total score ranging from 0 to 42; higher scores indicate worse bowel function (0-20: no LARS; 21-29: minor LARS; 30-42: major LARS).

6 months after surgery (3 months after stoma closure for participants whose protective stoma has not been closed by 6 months after surgery)

2차 결과 측정

결과 측정
측정값 설명
기간
LARS Score
기간: 6 months after surgery (3 months after stoma closure for participants whose protective stoma has not been closed by 6 months after surgery)

Total LARS score (range 0-42; higher scores indicate worse bowel function), compared between groups as a continuous variable.

6 months after surgery (3 months after stoma closure for participants whose protective stoma has not been closed by 6 months after surgery)
Serum Homocysteine Concentration
기간: Baseline (preoperative), and 3 and 6 months after surgery

Serum homocysteine concentration (μmol/L).

Baseline (preoperative), and 3 and 6 months after surgery
Systolic Blood Pressure
기간: 3 and 6 months after surgery

Systolic blood pressure (mmHg) measured in the seated position.

3 and 6 months after surgery
Diastolic Blood Pressure
기간: 3 and 6 months after surgery

Diastolic blood pressure (mmHg) measured in the seated position.

3 and 6 months after surgery
Anal Resting Pressure
기간: 3 and 6 months after surgery

Anal resting pressure (mmHg) measured by anorectal manometry.

3 and 6 months after surgery
Maximum Anal Squeeze Pressure
기간: 3 and 6 months after surgery

Maximum anal squeeze pressure (mmHg) measured by anorectal manometry.

3 and 6 months after surgery
Presence of Rectoanal Inhibitory Reflex
기간: 3 and 6 months after surgery

Proportion of participants with a present rectoanal inhibitory reflex on anorectal manometry.

3 and 6 months after surgery

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 수석 연구원: Wei Guo, MD, PhD, Qilu Hospital of Shandong University

간행물 및 유용한 링크

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일반 간행물

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 12월 1일

기본 완료 (추정된)

2027년 12월 1일

연구 완료 (추정된)

2027년 12월 1일

연구 등록 날짜

최초 제출

2026년 11월 4일

QC 기준을 충족하는 최초 제출

2026년 11월 4일

처음 게시됨 (실제)

2026년 11월 10일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 11월 10일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 11월 4일

마지막으로 확인됨

2026년 11월 1일

추가 정보

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아니요

IPD 계획 설명

Individual participant data are subject to China's Regulations on the Management of Human Genetic Resources and will not be shared publicly. De-identified data supporting the published results may be made available upon reasonable request to the principal investigator, subject to approval by Qilu Hospital of Shandong University and compliance with applicable Chinese regulations.

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