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| Name | Class |
|---|---|
| Hohhot First Hospital | UNKNOWN |
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This is a future-proof and randomized controlled clinical study on the clinical efficacy of graphene photothermal adjuvant therapy in Corona Virus Disease 2019(COVID-19) patients with mild symptoms. The objective is to examine the effect of graphene photothermal adjuvant therapy on the time line for such Corona Virus Disease 2019 patients to achieve a negative severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) nucleic acid test result, and their duration of disease. Patients who meet study criteria will be randomized into the Grapheme adjuvant therapy combined with conventional therapy group (treatment group) and the conventional therapy only group (control group). Contrasted to the control groups, the treatment groups will undergo 30-min of graphene adjuvant therapy every day for 7 d.
Following enrollment, patients will be randomized into treatment or control groups. All groups will receive the same conventional therapy.
In addition, treatment groups will undergo Graphene adjuvant therapy 30 minutes per day for 7 d.
Upon completion of the treatment protocol, specific study endpoints will be compared between the treatment and control groups.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Graphene adjuvant therapy combined with conventional therapy group (treatment group) | Experimental | Graphene adjuvant therapy combined with conventional therapy group (treatment group):Contrasted to the control groups, the treatment groups will undergo 30-min of graphene adjuvant therapy every day for 7 d. |
|
| Conventional therapy group (control group) | No Intervention | Conventional therapy group (control group):Patients will only receive the conventional treatment for COVID-19. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Graphene spectrum light wave therapy room | Device | Undergo 30-min of graphene adjuvant therapy every day for 7 d. |
|
| Measure | Description | Time Frame |
|---|---|---|
| The time from positive at baseline to negative SARS-CoV-2 nucleic acid test | The time for grouped patients to receive a negative SARS-CoV-2 nucleic acid test result, including both ORF gene Ct value≥35 and N gene Ct value≥35. | through study completion, an average of 10 days |
| Measure | Description | Time Frame |
|---|---|---|
| Hospital stay | Time to hospitalization for COVID-19 | through study completion, an average of 15 days |
| Negative test rate within 7 days | the rate of negative test of patients |
| Measure | Description | Time Frame |
|---|---|---|
| Lymphocytes variation | Lymphocytes count | through study completion, an average of 15 days |
Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Songqiao Liu, PhD. | Contact | 086-02583262550 | liusongqiao@ymail.com | |
| Junjing Zhang | Contact | 086-04175281618 | zhang.jj@vip.163.com |
| Name | Affiliation | Role |
|---|---|---|
| Songqiao Liu, PhD. | Southeast University | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Hohhot First Hospital | Recruiting | Hohhot | Inner Mongolia | 010031 | China |
We did not seek or receive approval for this data sharing from our Institutional Review Board .
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| ID | Term |
|---|---|
| D000086382 | COVID-19 |
| ID | Term |
|---|---|
| D011024 | Pneumonia, Viral |
| D011014 | Pneumonia |
| D012141 | Respiratory Tract Infections |
| D007239 | Infections |
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| 7 days |
| Mild to moderate rate within 14 days | Mild to moderate rate within 14 days | 14 days |
| D014777 |
| Virus Diseases |
| D018352 | Coronavirus Infections |
| D003333 | Coronaviridae Infections |
| D030341 | Nidovirales Infections |
| D012327 | RNA Virus Infections |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |