Covid19 and the mass feminisation of men

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Covid19 and the mass feminisation of men

In yet another blatant move toward the feminisation of men, a Californian based study has concluded that injecting the female sex hormone progesterone could improve outcomes for men hospitalised with Covid19.

The research was undertaken by pulmonologist Sara Ghandehari of the Cedars-Sinai hospital in Los Angeles and her colleagues.

'As an ICU doctor, I was struck by the gender disparity among COVID-19 patients who were very sick, remained in the hospital and needed ventilators,' she said. 

In their clinical trial, which was undertaken from April–August last year, the researchers recruited 40 male patients who had been hospitalised with moderate to severe COVID-19 and randomly divided them into two groups. 

One group acted as a control sample, for comparison, and received only the standard medical care given at that time for the disease.

The experimental group, meanwhile, also received 100 milligram injections of progesterone twice daily for five days during the time they were hospitalised.

All the patients were assessed by the team daily for either 15 days or until they were discharged from hospital.

The researchers found that, compared with the control group, patients who received the progesterone treatments scored a median of 1.5 points higher on the scale.

No short term serious adverse effects were observed as a result of the progesterone injections. Two patients did die during the 15-day study period — one from each of the two groups — but such were unrelated to the experiment treatments, the team said.

'While our findings are encouraging for the potential of using progesterone to treat men with COVID-19, our study had significant limitations,' cautioned Dr Ghandehari.

Firstly, she explained, the sample size was relatively small and was primarily made up of White, Hispanic and obese individuals with a moderate burden of other conditions, which serve to increase the risk of worse outcomes.

Furthermore, while the trial was randomised and featured a control group, it was also unblinded — meaning that the research team, physicians and patients all knew who had received the experimental treatment.  

'Further research is necessary in larger, more heterogeneous populations, including postmenopausal women and at other treatment centres,' Dr Ghandehari added.

This, she continued, will allow the team 'to establish the degree of clinical efficacy and to assess any other potential safety concerns of this treatment approach.'

 

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