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All Studies   All Outcomes    Recent:   
0 0.5 1 1.5 2+ Ventilation 84% Improvement Relative Risk ICU admission 76% Clinical improvement 67% CT improvement 73% Diathermy  Tian et al.  LATE TREATMENT  DB RCT Is late treatment with diathermy beneficial for COVID-19? Double-blind RCT 40 patients in China (March - April 2020) Improved recovery with diathermy (p=0.005) c19early.org Tian et al., European J. Physical and .., Mar 2022 Favors diathermy Favors control

Efficacy and safety of short-wave diathermy treatment for moderate COVID-19 patients: a prospective, double-blind, randomized controlled clinical study

Tian et al., European Journal of Physical and Rehabilitation Medicine, doi:10.23736/S1973-9087.21.06892-1
Mar 2022  
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42nd treatment shown to reduce risk in December 2023
 
*, now known with p = 0.026 from 4 studies.
Lower risk for recovery.
No treatment is 100% effective. Protocols combine complementary and synergistic treatments. * >10% efficacy in meta analysis with ≥3 clinical studies.
3,800+ studies for 60+ treatments. c19early.org
RCT 42 moderate COVID-19 inpatients showing significantly faster clinical and CT scan improvement with short-wave diathermy (SWD) treatment added to standard care, compared to placebo SWD plus standard care. 92.6% of the SWD group had clinical improvement at 14 days, compared to 69.2% in the control group. The SWD group also had significantly faster CT scan improvement. There was no significant difference in adverse events between groups, with only minor side effects like headache and dizziness reported.
risk of mechanical ventilation, 84.0% lower, RR 0.16, p = 0.09, treatment 1 of 27 (3.7%), control 3 of 13 (23.1%), NNT 5.2.
risk of ICU admission, 75.9% lower, RR 0.24, p = 0.07, treatment 2 of 27 (7.4%), control 4 of 13 (30.8%), NNT 4.3.
clinical improvement, 67.2% lower, HR 0.33, p = 0.005, treatment 27, control 13, inverted to make HR<1 favor treatment, Cox proportional hazards.
CT improvement, 73.1% lower, HR 0.27, p = 0.005, treatment 27, control 13, inverted to make HR<1 favor treatment, Cox proportional hazards.
Effect extraction follows pre-specified rules prioritizing more serious outcomes. Submit updates
Tian et al., 31 Mar 2022, Double Blind Randomized Controlled Trial, placebo-controlled, China, peer-reviewed, 12 authors, study period 1 March, 2020 - 5 April, 2020, diathermy. Contact: yuanhuafmmu@foxmail.com.
This PaperThermotherapyAll
Efficacy and safety of short-wave diathermy treatment for moderate COVID-19 patients: a prospective, double-blind, randomized controlled clinical study
Fei Tian, Jin Wang, Xiao Xi, Xiaolong Sun, Miao He, Chenguang Zhao, Feng Feng, Hongbin Wang, Wei Sun, Li Mao, Xu Hu, Hua Yuan
doi:10.23736/S1973-9087.21.06892-1)
BACKGROUND: Millions of human beings have suffered in the epidemic of Coronavirus disease 2019 (COVID-19), but until now the effective treatment methods have been limited. AIM: This study aimed to evaluate the efficacy and safety of short-wave diathermy (SWD) treatment for moderate COVID-19 patients. DESIGN: A prospective, double-blind, randomized controlled clinical study. SETTING: Inpatients Unit of a COVID-19 specialized hospital. POPULATION: Forty-two patients with moderate COVID-19 were randomly allocated at a 2:1 ratio to two groups: the SWD group and the control group. METHODS: Participants of the SWD group received SWD treatment, and participants of the control group received placebo SWD treatment for one session per day, 10 minutes per session, for no more than 14 days. Both groups were given standard care treatment. Primary outcome was the rate of clinical improvement according to a seven-category ordinal scale. Secondary outcomes included the rate of computed tomography (CT) improvement and the rate of potential adverse events. RESULTS: Clinical improvement occurred in 92.6% of patients in the SWD group by day 14 compared with 69.2% of patients in the control group (P=0.001). The Cox model indicated that the SWD group had a higher clinical improvement probability than the control group (hazard ratio: 3.045; 95% CI: 1.391-6.666; P=0.005). Similarly, CT improvement occurred in 85.2% of patients in the SWD group and 46.2% of patients in the control group respectively by day 14 (P=0.001). The Cox model indicated SWD group had a higher CT improvement probability than control group (hazard ratio: 3.720; 95% CI: 1.486-9.311; P=0.005). There was no significant difference in adverse events between the SWD group and the control group (2 of 27 [7.4%] SWD vs. 1 of 13 [7.7%] control, P=1.000), the most frequent of which were headache (1 of 27 [3.7%] SWD vs. 1 of 13 [7.7%] control patients) and dizziness (1 of 27 [3.7%] SWD vs. 0 of 13 [0%] control patients). CONCLUSIONS: SWD is a valid and reliable adjuvant therapy with a favorable safety profile for moderate COVID-19 patients. CLINICAL REHABILITATION IMPACT: Clinically relevant information is lacking regarding the efficacy and safety of SWD for patients with COVID-19. This study provides the first evidence that SWD is a promising adjuvant therapy for COVID-19.
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Late treatment
is less effective
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