Before the treatment

Find some basic questions about the process

To access the services of Iuvenis Clinic, is it essential to undergo a prior assessment?

Yes, every individual must be evaluated by professionals. We need to know their medical history, verify their current condition, and based on that, we will communicate the feasibility of the process.

Where are the treatments conducted?

Our headquarters in Panama City is available to welcome international patients who are seeking scientific alternatives for themselves or their family members.

Are there places to stay in Panama City?

We have established partnerships with major hotel chains that are located near our facilities, making transportation during the treatment period convenient.

Can I coordinate my accommodation directly?

Each patient can arrange their transportation and accommodation independently, choosing the sites they consider best. Iuvenis Clinic provides options that have been evaluated for the quality of service and proximity to our facilities. If the patient arranges accommodation independently, it is essential to verify distances and logistical details to meet the appointment times. Iuvenis does not assume responsibility for aspects related to patient accommodation; it only suggests some alternatives to facilitate the person’s stay.

How is the start of treatments confirmed?

Once the team of professionals at Iuvenis Clinic has assessed the information provided through the official forms, treatment approval is obtained through the respective documents sent to the patient or their responsible family members. The associated costs will be communicated, and upon confirmation of financial transfers, the start of treatments will be confirmed.

About the treatment

Most of the questions patients have about the stem cells treatment

The delivery of stem cells at Stem Cell Institute varies depending on the patient’s condition. Typically, a minimum of three applications is administered throughout the treatment protocol. Methods include Intravenous (IV), intramuscular, intrathecal, and perilymphatic.

To initiate the evaluation process, interested individuals can complete the Patient Application that will be sent to your personal email. For inquiries, please contact us directly.

Cord donations from healthy women in Panama who have undergone normal births supply our stem cells. Donors undergo a thorough process, including signing a consent form, completing a detailed questionnaire, and providing a blood sample. Rigorous testing for HIV, STDs, hepatitis, etc., is conducted on the donated blood.

Results vary among patients, and there is no guaranteed timeframe for positive outcomes. Some patients report improvements during treatment, while others experience progress up to six months after returning home. However, not all patients show improvement.

Protocols differ based on the disease, considering the patient’s physical condition and other medical factors. Most protocols span 3-5 days, consisting of 3-4 sessions. Contact us for information on conditions we treat.

Generally, beyond initial injection site discomfort, patients experience minimal discomfort. Less than 10% of patients, mainly those undergoing lumbar puncture, may develop temporary symptoms such as fever, headache, nausea, or vomiting, lasting no more than three days, typically resolving within 24 hours. No long-term negative effects have been reported.

Physical therapy may be recommended for specific treatment protocols and provided during the course of treatment. Generally, no medication is prescribed as part of the treatment. However, a post-treatment stem cell enhancing supplement regime may be advised.

Normally, physicians do not issue any medication as part of your treatment. Nevertheless, they might recommend a regimen of circulating stem cell enhancing supplements after the completion of the treatment.

Smoking and drinking can adversely affect new progenitor stem cells. It is recommended to refrain from smoking or drinking during treatments.

Service fees begin at $15,000 USD for children and $25,000 for adults. Costs depend on the recommended protocol and are provided in writing upon approval. The fee covers the treatment. Costs related to hotel room, food, communications and transportation are not involved.

Stem cell therapy is not covered by insurance companies, especially when conducted in foreign countries.

Adult stem cells, distinct from fetal and embryonic stem cells, avoid associated controversies. Both the Catholic Church and the Southern Baptist Church endorse the use of adult stem cells as an ethically acceptable alternative.

No stem cell product for our treated conditions is approved by the US FDA. However, mesenchymal stem cells derived from human umbilical cord tissue, isolated and grown in our Panama laboratory, have been utilized in the US under FDA regulation for clinical trials. These cells were used in a compassionate use case for two Duchenne’s muscular dystrophy patients under the FDA’s Investigational New Drug designation. (IND 16026 DMD Single Patient).

Through our contact channels, we can address your concerns. Write to us through our official email, or you can ask relevant questions if your case involves a call with one of our advisors.

Have additional questions?

We’re here to help. Let’s talk.