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Phytochemical study and development of human supplementation based on biochemical exams with a standardized extract of watercress

Phytochemical study and development of human supplementation based on biochemical parameters with a standardized extract of Nasturtium officinale R.Br. Brassicaceae

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-4rhbpq
Enrollment
Unknown
Registered
2019-10-10
Start date
2018-04-08
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Escherichia coli infection

Interventions

supplemented group: 45 individuals with physical disabilities supplemented with 750mg /kg/d of standardized watercress extract for 35 days. Control group: 45 individuals with physical disability su
Other
B01.650.940.800.575.912.250.157.644
E02.190.755
B01.650.940.800.575.912.250.157

Sponsors

Universidade Federal do Pararna
Lead Sponsor
Universidade Federal do Pararna
Collaborator

Eligibility

Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Volunteers with a physical disability, such as spinal cord injury; cerebral palsy and amputated; aged between 18 and 65 years old; para-sport practicer; being a member of Physical disability of Parana.

Exclusion criteria

Exclusion criteria: Volunteers using cholesterol, diabetes, antibiotics and anti-inflammatory drugs

Design outcomes

Primary

MeasureTime frame
Outcome 1It was observed immune parameters related to urinary infections in the studied population through type 1 urine tests and complete blood count.;Outcome 1: No improvement in immune parameters related to urinary tract infections was found.;Outcome 2: I was observed oxidative stress parameter through the methods of TBARS, PC, CAT, SOD, and GSH, in the blood;Outocme 2: Improved oxidative stress studies were found in the TBARS, PC, CAT, and SOD studies, and no statistical differences in GSH.;Outcome 3: Inflammatory system will be observed in patients with physical disabilities through the method of inflammatory mediators in the blood

Secondary

MeasureTime frame
There were no secondary outcomes found to date.

Countries

Brazil

Contacts

Public ContactMirna Clemente

Universidade Federal do Pararna

mirnaclemente@yahoo.com+554133604098

Outcome results

None listed

Source: REBEC (via WHO ICTRP)