Beijing Di Tan Hospital, , Capital Medical University
Beijing, China, 102488
Location status: Recruiting
NCT Number: NCT06980636
The goal of this clinical trial is to learn if Shengmai liquid works to treat Long Covid fatigue. It will also learn about the safety of Shengmai liquid. The main questions it aims to answer are:
* Dose the Shengmai liquid will reduce the level of fatigue in the participants and reduce the fatigue scale score of the participants? * Dose the Shengmai liquid will reduce the level of anxiety and depression in the participants and improve the sleep quality and quality of life of the participants Researchers will compare Shengmai oral liquid to a placebo (a look-alike substance that contains no drug) to see if Shengmai liquid works to treat Long Covid fatigue.
Participants will:
* Take Shengmai liquid or a placebo every day for 8 weeks. * Visit the clinic once every 4 weeks for check up and test. There are a total of two telephone follow-ups, one follow-up 15 days after the treatment starts and another follow-up 30 days after the treatment ends. * Participants' medication responses and scale scores will be recorded.
Interested in participating?
Request Info18 year–75 year
All sexes
Interventional
Phase 4
Beijing, China, 102488
Location status: Recruiting
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The Shengmaiyin treatment group will be given the traditional Chinese medicine Shengmaiyin oral liquid (produced by Jilin Aodong Yanbian Pharmaceutical Co., Ltd., with the approval number Z41021384. Ingredients: Codonopsis pilosula, Ophiopogon japonicus, Schisandra chinensis, excipients: sucrose, sodium benzoate, ethylparaben, specification 10m1/bottle), taken orally at a dose of 10ml per time, three times a day
A simulated Shengmaiyin oral liquid (provided by Jilin Aodong Yanbian Pharmaceutical Co., Ltd., with main ingredients water, brown sugar, flavoring agents, etc., specification 10m/bottle), 10ml per time, three times a day. The treatment course for Shengmaiyin or placebo will be 8 weeks (56 days), with follow-up continuing until 30 days after the end of the treatment course.
Time frame: From enrollment to the end of follow up at 12 weeks
MFIS is a standardized questionnaire reflecting physical and mental fatigue, consisting of 21 questions. Each question has five options (none at all, a little, sometimes, often, almost always), with a total score range of 0 to 84. The higher the score, the higher the degree of chronic fatigue.
Time frame: From enrollment to the end of treatment at 8 week
Measured once during the screening period before the start of the trial, and then at 30 days and 60 days during the trial, for a total of three measurements.
Time frame: From enrollment to the end of treatment at 8 weeks
Measured once during the screening period before the start of the trial, and then at 30 days and 60 days during the trial, for a total of three measurements.
Time frame: From enrollment to the end of treatment at 8 weeks
Measured once during the screening period before the start of the trial, and then at 30 days and 60 days during the trial, for a total of three measurements.
Time frame: From enrollment to the end of treatment at 8 week
Measured once during the screening period before the start of the trial, and then at 30 days and 60 days during the trial, for a total of three measurements.
Time frame: From enrollment to the end of treatment at 8 weeks
measured once during the screening period before the start of the trial, and then at 30 days and 60 days during the trial, for a total of three measurements.
Time frame: From enrollment to the end of treatment at 8 weeks
Measured once during the screening period before the start of the trial, and then at 30 days and 60 days during the trial, for a total of three measurements.
Contact information is provided by the study sponsor or research team.
Beijing University of Chinese Medicine
Other
Shengmai Liquid for Long COVID Fatigue: a Randomized Placebo-controlled Trial.
Acronym: Shengmai LOFT
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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