跳至主要内容
临床试验/NCT05451927
NCT05451927已完成不适用

A Randomized Double Blind Study to Examine the Effect of Natural Anti-obesity Agent Among Women of Lahore

Hafiza Aisha Sadiqa2 个研究点 分布在 1 个国家目标入组 72 人开始时间: 2022年10月27日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
72
试验地点
2
主要终点
Body weight

研究概览

简要总结

This double-blind randomized placebo-controlled trial will test the hypothesis that administration of Phaseolus Vulgaris supplementation to women in Lahore, Pakistan, who are overweight will induce the weight loss (Primary outcome) and changes in body composition (Waist circumference) secondary outcome.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者
是

入选标准

  • •BMI ranges from 25-40
  • •Consistently stable body weight for at least 6 months
  • •Good general health
  • •No ongoing drug treatment for weight reduction
  • •Commitment to avoid any changes in lifestyle throughout the test period
  • •Age between 18-45 years
  • •Women resident of Lahore

排除标准

  • •Pregnant or breast-feeding females
  • •People with Type 2 diabetes
  • •People with any other chronic diseases
  • •Weight reduction treatment during the 6 months prior to the study

研究组 & 干预措施

Placebo

Placebo Comparator

Three oral doses of Placebo daily for 3 months

干预措施: Placebo (Dietary Supplement)

Phaseolus Vulgaris

Experimental

Three oral doses of 1000 mg Phaseolus Vulgaris daily for 3 months

干预措施: Phaseolus Vulgaris (Dietary Supplement)

结局指标

主要结局

Body weight

时间窗: 3 months

change in body weight

次要结局

未报告次要终点

研究者

发起方
Hafiza Aisha Sadiqa
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Hafiza Aisha Sadiqa

Student

University of the Punjab

研究点 (2)

Loading locations...

相似试验

尚未招募
不适用
A study to measure markers in the breath of patients with Chronic Obstructive Pulmonary Disease (COPD)Respiratory - Chronic obstructive pulmonary diseaseChronic Obstructive Pulmonary Disease
ACTRN12614000617662ung Institute of Western Australia200
进行中(未招募)
1 期
Effect of testosterone in male patients on regular hemodialysisHypogonadal males undergoing hemodialysis (HD).
EUCTR2011-005439-20-SEDept of Renal medicine40
进行中(未招募)
不适用
A randomised, double-blind study to assess the efficacy and safety of prophylactis use of maribavir versus oral ganciclovir for the prevention of cytomegalovirus disease in recipients of orthotopic liver transplants - NDPatient undergone to orthotopic liver transplantsMedDRA version: 9.1Level: LLTClassification code 10011831Term: Cytomegalovirus infection
EUCTR2007-004729-16-ITVIROPHARMA INCORPORATED348
进行中(未招募)
1 期
Randomised, double-blind study to demonstrate therapeutic equivalence of formoterol fumarate 12µg capsules delivered by Cyclohaler with Foradil in mild to moderate reversible obstructive airways disease.mild to moderate reversible obstructive airways disease
EUCTR2005-002538-37-GBPharmachemie B.V.30
进行中(未招募)
1 期
A double blind, placebo controlled study to evaluate the safety and immunogenicity of escalating doses of 108 CFU, 109 CFU and 1010 CFU of M04NM11 in patients who have chronic Hepatitis B infection. - Not AvailableChronic hepatitis B virus infection
EUCTR2005-005293-70-GBEmergent Product Development UK Ltd45