Clinical trials

Ability to confirm voluntary participation and agreement with all study objectiv... [+5]

Use of prednisolone or any other oral or parenteral corticosteroid within 7 days... [+18]

Participant must be 18 years of age or older at the time of signing the informed... [+12]

Any clinical observation (clinical/physical assessment) or laboratory condition... [+32]

Patient has given written informed consent to participate in the study prior to... [+4]

Diagnosis of secondary dysmenorrhea; [+26]

Ability to confirm voluntary participation and agree to all trial purposes by si... [+1]

Any clinical and laboratory findings that, in the judgment of the investigator,... [+5]

Ability to confirm voluntary participation and agree to all trial purposes by si... [+4]

Any clinical and laboratory findings that, in the judgment of the investigator,... [+19]

Ability to confirm voluntary participation and agree to all trial purposes by si... [+5]

Any clinical and laboratory findings that, in the judgment of the investigator,... [+22]

Ability to confirm voluntary participation and agree to all trial purposes by si... [+1]

Known hypersensitivity to the formula components used during the clinical trial; [+10]

Ability to confirm voluntary participation and agree to all trial purposes by si... [+9]

Known hypersensitivity to the formula components used during the clinical trial; [+13]

Patient has given written informed consent to participate in the study before ad... [+4]

Diagnosis of secondary dysmenorrhea; [+24]

Ability to confirm voluntary participation and agree for all the purposes of the... [+5]

Use of prednisolone or other oral or parenteral corticosteroid in the seven (07)... [+10]

Patient has given written informed consent to participate in the study prior to... [+4]

Diagnosis of secondary dysmenorrhea; [+23]

men aged 40 years and older. [+4]

Any clinical or physical observation noted during evaluation by the investigatin... [+27]

Ability to confirm voluntary participation and agree with all the purposes of th... [+3]

Presence of local conditions (lesions in the region of the third molars) that ma... [+23]

Ability to confirm voluntary participation and agree to all trial purposes by si... [+3]

Any clinical or physical finding interpreted by the investigator as a risk to su... [+22]

Ability to confirm voluntary participation and agree to all trial purposes by si... [+3]

Any clinical observation or laboratory condition finding that is interpreted by... [+23]

Ability to confirm voluntary participation and agree to all trial purposes by si... [+7]

Any clinical and laboratory findings that, in the judgment of the investigator,... [+8]